Canonical Allele Identifier: CA2761715254

Gene: KIT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54736621_54736773del , CM000666.2:g.54736621_54736773del	GRCh38
NC_000004.11:g.55602787_55602939del , CM000666.1:g.55602787_55602939del	GRCh37
NC_000004.10:g.55297544_55297696del	NCBI36
NG_007456.1:g.83627_83779del , LRG_307:g.83627_83779del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.2584+12_2637del
ENST00000684818.1:n.1288+12_1341del
ENST00000685269.1:n.2674+12_2727del
ENST00000686011.1:c.2581+12_2634del
ENST00000687109.1:c.2599+12_2652del
ENST00000687208.1:n.3008+12_3061del
ENST00000687246.1:c.2461+12_2514del
ENST00000687265.1:n.2754+12_2807del
ENST00000687295.1:c.2584+12_2637del
ENST00000688060.1:n.393+12_446del
ENST00000689832.1:c.2596+12_2649del
ENST00000689994.1:c.2086+12_2139del
ENST00000690543.1:c.2587+12_2640del
ENST00000690917.1:n.2814+12_2867del
ENST00000691361.1:n.1506+12_1559del
ENST00000692301.1:n.1288+12_1341del
ENST00000692783.1:c.2593+12_2646del
ENST00000692991.1:n.2693+12_2746del
ENST00000288135.6:c.2596+12_2649del
ENST00000288135.5:c.2596+12_2649del
ENST00000412167.6:c.2584+12_2637del
NM_000222.2:c.2596+12_2649del , LRG_307t1:c.2596+12_2649del
NM_001093772.1:c.2584+12_2637del
XM_005265740.1:c.2599+12_2652del
XM_005265741.1:c.2596+12_2649del
XM_005265742.1:c.2587+12_2640del
XM_005265742.3:c.2587+12_2640del
XM_017008178.1:c.2593+12_2646del
XM_017008179.1:c.2584+12_2637del
XM_017008180.1:c.2581+12_2634del
NM_000222.3:c.2596+12_2649del
NM_001093772.2:c.2584+12_2637del
NM_001385284.1:c.2599+12_2652del
NM_001385285.1:c.2593+12_2646del
NM_001385286.1:c.2581+12_2634del
NM_001385288.1:c.2587+12_2640del
NM_001385290.1:c.2596+12_2649del
NM_001385292.1:c.2584+12_2637del