Canonical Allele Identifier: CA356911408

Gene: KIT

Linked Data

• MyVariant Identifiers: chr4:g.55599248G>T (hg19) ; chr4:g.54733082G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54733082G>T , CM000666.2:g.54733082G>T	GRCh38
NC_000004.11:g.55599248G>T , CM000666.1:g.55599248G>T	GRCh37
NC_000004.10:g.55294005G>T	NCBI36
NG_007456.1:g.80088G>T , LRG_307:g.80088G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000412167.7:c.2362G>T	ENSP00000390987.3:p.Asp788Tyr
ENST00000685269.1:n.2452G>T
ENST00000686011.1:c.2359G>T	ENSP00000509704.1:p.Asp787Tyr
ENST00000687109.1:c.2377G>T	ENSP00000509371.1:p.Asp793Tyr
ENST00000687208.1:n.2786G>T
ENST00000687246.1:c.2349+1084G>T	ENSP00000509114.1:n.2349+1084G>T
ENST00000687265.1:n.2532G>T
ENST00000687295.1:c.2362G>T	ENSP00000509450.1:p.Asp788Tyr
ENST00000688060.1:n.171G>T
ENST00000688704.1:n.1386G>T
ENST00000689832.1:c.2374G>T	ENSP00000509084.1:p.Asp792Tyr
ENST00000689994.1:c.1864G>T	ENSP00000509156.1:p.Asp622Tyr
ENST00000690543.1:c.2365G>T	ENSP00000508831.1:p.Asp789Tyr
ENST00000690917.1:n.2592G>T
ENST00000691361.1:n.1284G>T
ENST00000692783.1:c.2371G>T	ENSP00000508733.1:p.Asp791Tyr
ENST00000692991.1:n.2471G>T
ENST00000288135.6:c.2374G>T MANE Select	ENSP00000288135.6:p.Asp792Tyr
ENST00000288135.5:c.2374G>T	ENSP00000288135.5:p.Asp792Tyr
ENST00000412167.6:c.2362G>T	ENSP00000390987.2:p.Asp788Tyr
ENST00000512959.1:n.427G>T
NM_000222.2:c.2374G>T , LRG_307t1:c.2374G>T	NP_000213.1:p.Asp792Tyr
NM_001093772.1:c.2362G>T	NP_001087241.1:p.Asp788Tyr
XM_005265740.1:c.2377G>T	XP_005265797.1:p.Asp793Tyr
XM_005265741.1:c.2374G>T	XP_005265798.1:p.Asp792Tyr
XM_005265742.1:c.2365G>T	XP_005265799.1:p.Asp789Tyr
XM_005265742.3:c.2365G>T	XP_005265799.1:p.Asp789Tyr
XM_017008178.1:c.2371G>T	XP_016863667.1:p.Asp791Tyr
XM_017008179.1:c.2362G>T	XP_016863668.1:p.Asp788Tyr
XM_017008180.1:c.2359G>T	XP_016863669.1:p.Asp787Tyr
NM_000222.3:c.2374G>T MANE Select	NP_000213.1:p.Asp792Tyr
NM_001093772.2:c.2362G>T	NP_001087241.1:p.Asp788Tyr
NM_001385284.1:c.2377G>T	NP_001372213.1:p.Asp793Tyr
NM_001385285.1:c.2371G>T	NP_001372214.1:p.Asp791Tyr
NM_001385286.1:c.2359G>T	NP_001372215.1:p.Asp787Tyr
NM_001385288.1:c.2365G>T	NP_001372217.1:p.Asp789Tyr
NM_001385290.1:c.2374G>T	NP_001372219.1:p.Asp792Tyr
NM_001385292.1:c.2362G>T	NP_001372221.1:p.Asp788Tyr