Canonical Allele Identifier: CA2761703022

Gene: KIT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54726362_54726363insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT , CM000666.2:g.54726362_54726363insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT	GRCh38
NC_000004.11:g.55592528_55592529insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT , CM000666.1:g.55592528_55592529insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT	GRCh37
NC_000004.10:g.55287285_55287286insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT	NCBI36
NG_007456.1:g.73368_73369insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT , LRG_307:g.73368_73369insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.1531+324_1531+325insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT	ENSP00000390987.3:n.1531+324_1531+325insGTTTGCTGGAGGTCCACTCCA...
ENST00000685269.1:n.1618+312_1618+313insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT
ENST00000686011.1:c.1528+324_1528+325insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT	ENSP00000509704.1:n.1528+324_1528+325insGTTTGCTGGAGGTCCACTCCA...
ENST00000687109.1:c.1543+312_1543+313insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT	ENSP00000509371.1:n.1543+312_1543+313insGTTTGCTGGAGGTCCACTCCA...
ENST00000687208.1:n.1955+312_1955+313insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT
ENST00000687246.1:c.1528+324_1528+325insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT	ENSP00000509114.1:n.1528+324_1528+325insGTTTGCTGGAGGTCCACTCCA...
ENST00000687265.1:n.1698+324_1698+325insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT
ENST00000687295.1:c.1528+324_1528+325insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT	ENSP00000509450.1:n.1528+324_1528+325insGTTTGCTGGAGGTCCACTCCA...
ENST00000689832.1:c.1543+312_1543+313insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT	ENSP00000509084.1:n.1543+312_1543+313insGTTTGCTGGAGGTCCACTCCA...
ENST00000689994.1:c.1030+312_1030+313insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT	ENSP00000509156.1:n.1030+312_1030+313insGTTTGCTGGAGGTCCACTCCA...
ENST00000690543.1:c.1531+324_1531+325insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT	ENSP00000508831.1:n.1531+324_1531+325insGTTTGCTGGAGGTCCACTCCA...
ENST00000690917.1:n.1758+312_1758+313insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT
ENST00000691361.1:n.450+324_450+325insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT
ENST00000692783.1:c.1540+312_1540+313insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT	ENSP00000508733.1:n.1540+312_1540+313insGTTTGCTGGAGGTCCACTCCA...
ENST00000692991.1:n.1637+324_1637+325insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT
ENST00000288135.6:c.1540+312_1540+313insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT MANE Select	ENSP00000288135.6:n.1540+312_1540+313insGTTTGCTGGAGGTCCACTCCA...
ENST00000288135.5:c.1540+312_1540+313insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT	ENSP00000288135.5:n.1540+312_1540+313insGTTTGCTGGAGGTCCACTCCA...
ENST00000412167.6:c.1528+324_1528+325insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT	ENSP00000390987.2:n.1528+324_1528+325insGTTTGCTGGAGGTCCACTCCA...
NM_000222.2:c.1540+312_1540+313insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT , LRG_307t1:c.1540+312_1540+313insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT	NP_000213.1:n.1540+312_1540+313insGTTTGCTGGAGGTCCACTCCATATCCT...
NM_001093772.1:c.1528+324_1528+325insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT	NP_001087241.1:n.1528+324_1528+325insGTTTGCTGGAGGTCCACTCCATAT...
XM_005265740.1:c.1543+312_1543+313insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT	XP_005265797.1:n.1543+312_1543+313insGTTTGCTGGAGGTCCACTCCATAT...
XM_005265741.1:c.1543+312_1543+313insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT	XP_005265798.1:n.1543+312_1543+313insGTTTGCTGGAGGTCCACTCCATAT...
XM_005265742.1:c.1531+324_1531+325insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT	XP_005265799.1:n.1531+324_1531+325insGTTTGCTGGAGGTCCACTCCATAT...
XM_005265742.3:c.1531+324_1531+325insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT	XP_005265799.1:n.1531+324_1531+325insGTTTGCTGGAGGTCCACTCCATAT...
XM_017008178.1:c.1540+312_1540+313insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT	XP_016863667.1:n.1540+312_1540+313insGTTTGCTGGAGGTCCACTCCATAT...
XM_017008179.1:c.1531+324_1531+325insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT	XP_016863668.1:n.1531+324_1531+325insGTTTGCTGGAGGTCCACTCCATAT...
XM_017008180.1:c.1528+324_1528+325insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT	XP_016863669.1:n.1528+324_1528+325insGTTTGCTGGAGGTCCACTCCATAT...
NM_000222.3:c.1540+312_1540+313insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT MANE Select	NP_000213.1:n.1540+312_1540+313insGTTTGCTGGAGGTCCACTCCATATCCT...
NM_001093772.2:c.1528+324_1528+325insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT	NP_001087241.1:n.1528+324_1528+325insGTTTGCTGGAGGTCCACTCCATAT...
NM_001385284.1:c.1543+312_1543+313insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT	NP_001372213.1:n.1543+312_1543+313insGTTTGCTGGAGGTCCACTCCATAT...
NM_001385285.1:c.1540+312_1540+313insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT	NP_001372214.1:n.1540+312_1540+313insGTTTGCTGGAGGTCCACTCCATAT...
NM_001385286.1:c.1528+324_1528+325insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT	NP_001372215.1:n.1528+324_1528+325insGTTTGCTGGAGGTCCACTCCATAT...
NM_001385288.1:c.1531+324_1531+325insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT	NP_001372217.1:n.1531+324_1531+325insGTTTGCTGGAGGTCCACTCCATAT...
NM_001385290.1:c.1543+312_1543+313insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT	NP_001372219.1:n.1543+312_1543+313insGTTTGCTGGAGGTCCACTCCATAT...
NM_001385292.1:c.1531+324_1531+325insGTTTGCTGGAGGTCCACTCCATATCCTGTTTGTCTGGGTATT	NP_001372221.1:n.1531+324_1531+325insGTTTGCTGGAGGTCCACTCCATAT...