Canonical Allele Identifier: CA356913176

Gene: KIT

Linked Data

• dbSNP Id: rs121913687
• MyVariant Identifiers: chr4:g.55602718A>T (hg19) ; chr4:g.54736552A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54736552A>T , CM000666.2:g.54736552A>T	GRCh38
NC_000004.11:g.55602718A>T , CM000666.1:g.55602718A>T	GRCh37
NC_000004.10:g.55297475A>T	NCBI36
NG_007456.1:g.83558A>T , LRG_307:g.83558A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.2527A>T	ENSP00000390987.3:p.Thr843Ser
ENST00000684818.1:n.1231A>T
ENST00000685269.1:n.2617A>T
ENST00000686011.1:c.2524A>T	ENSP00000509704.1:p.Thr842Ser
ENST00000687109.1:c.2542A>T	ENSP00000509371.1:p.Thr848Ser
ENST00000687208.1:n.2951A>T
ENST00000687246.1:c.2404A>T	ENSP00000509114.1:p.Thr802Ser
ENST00000687265.1:n.2697A>T
ENST00000687295.1:c.2527A>T	ENSP00000509450.1:p.Thr843Ser
ENST00000688060.1:n.336A>T
ENST00000689832.1:c.2539A>T	ENSP00000509084.1:p.Thr847Ser
ENST00000689994.1:c.2029A>T	ENSP00000509156.1:p.Thr677Ser
ENST00000690543.1:c.2530A>T	ENSP00000508831.1:p.Thr844Ser
ENST00000690917.1:n.2757A>T
ENST00000691361.1:n.1449A>T
ENST00000692301.1:n.1231A>T
ENST00000692783.1:c.2536A>T	ENSP00000508733.1:p.Thr846Ser
ENST00000692991.1:n.2636A>T
ENST00000288135.6:c.2539A>T MANE Select	ENSP00000288135.6:p.Thr847Ser
ENST00000288135.5:c.2539A>T	ENSP00000288135.5:p.Thr847Ser
ENST00000412167.6:c.2527A>T	ENSP00000390987.2:p.Thr843Ser
NM_000222.2:c.2539A>T , LRG_307t1:c.2539A>T	NP_000213.1:p.Thr847Ser
NM_001093772.1:c.2527A>T	NP_001087241.1:p.Thr843Ser
XM_005265740.1:c.2542A>T	XP_005265797.1:p.Thr848Ser
XM_005265741.1:c.2539A>T	XP_005265798.1:p.Thr847Ser
XM_005265742.1:c.2530A>T	XP_005265799.1:p.Thr844Ser
XM_005265742.3:c.2530A>T	XP_005265799.1:p.Thr844Ser
XM_017008178.1:c.2536A>T	XP_016863667.1:p.Thr846Ser
XM_017008179.1:c.2527A>T	XP_016863668.1:p.Thr843Ser
XM_017008180.1:c.2524A>T	XP_016863669.1:p.Thr842Ser
NM_000222.3:c.2539A>T MANE Select	NP_000213.1:p.Thr847Ser
NM_001093772.2:c.2527A>T	NP_001087241.1:p.Thr843Ser
NM_001385284.1:c.2542A>T	NP_001372213.1:p.Thr848Ser
NM_001385285.1:c.2536A>T	NP_001372214.1:p.Thr846Ser
NM_001385286.1:c.2524A>T	NP_001372215.1:p.Thr842Ser
NM_001385288.1:c.2530A>T	NP_001372217.1:p.Thr844Ser
NM_001385290.1:c.2539A>T	NP_001372219.1:p.Thr847Ser
NM_001385292.1:c.2527A>T	NP_001372221.1:p.Thr843Ser