Canonical Allele Identifier: CA439291822

Gene: KIT

Linked Data

• MyVariant Identifiers: chr4:g.55599251T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54733085T>C , CM000666.2:g.54733085T>C	GRCh38
NC_000004.11:g.55599251T>C , CM000666.1:g.55599251T>C	GRCh37
NC_000004.10:g.55294008T>C	NCBI36
NG_007456.1:g.80091T>C , LRG_307:g.80091T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000412167.7:c.2365T>C	ENSP00000390987.3:p.Leu789=
ENST00000685269.1:n.2455T>C
ENST00000686011.1:c.2362T>C	ENSP00000509704.1:p.Leu788=
ENST00000687109.1:c.2380T>C	ENSP00000509371.1:p.Leu794=
ENST00000687208.1:n.2789T>C
ENST00000687246.1:c.2349+1087T>C	ENSP00000509114.1:n.2349+1087T>C
ENST00000687265.1:n.2535T>C
ENST00000687295.1:c.2365T>C	ENSP00000509450.1:p.Leu789=
ENST00000688060.1:n.174T>C
ENST00000688704.1:n.1389T>C
ENST00000689832.1:c.2377T>C	ENSP00000509084.1:p.Leu793=
ENST00000689994.1:c.1867T>C	ENSP00000509156.1:p.Leu623=
ENST00000690543.1:c.2368T>C	ENSP00000508831.1:p.Leu790=
ENST00000690917.1:n.2595T>C
ENST00000691361.1:n.1287T>C
ENST00000692783.1:c.2374T>C	ENSP00000508733.1:p.Leu792=
ENST00000692991.1:n.2474T>C
ENST00000288135.6:c.2377T>C MANE Select	ENSP00000288135.6:p.Leu793=
ENST00000288135.5:c.2377T>C	ENSP00000288135.5:p.Leu793=
ENST00000412167.6:c.2365T>C	ENSP00000390987.2:p.Leu789=
ENST00000512959.1:n.430T>C
NM_000222.2:c.2377T>C , LRG_307t1:c.2377T>C	NP_000213.1:p.Leu793=
NM_001093772.1:c.2365T>C	NP_001087241.1:p.Leu789=
XM_005265740.1:c.2380T>C	XP_005265797.1:p.Leu794=
XM_005265741.1:c.2377T>C	XP_005265798.1:p.Leu793=
XM_005265742.1:c.2368T>C	XP_005265799.1:p.Leu790=
XM_005265742.3:c.2368T>C	XP_005265799.1:p.Leu790=
XM_017008178.1:c.2374T>C	XP_016863667.1:p.Leu792=
XM_017008179.1:c.2365T>C	XP_016863668.1:p.Leu789=
XM_017008180.1:c.2362T>C	XP_016863669.1:p.Leu788=
NM_000222.3:c.2377T>C MANE Select	NP_000213.1:p.Leu793=
NM_001093772.2:c.2365T>C	NP_001087241.1:p.Leu789=
NM_001385284.1:c.2380T>C	NP_001372213.1:p.Leu794=
NM_001385285.1:c.2374T>C	NP_001372214.1:p.Leu792=
NM_001385286.1:c.2362T>C	NP_001372215.1:p.Leu788=
NM_001385288.1:c.2368T>C	NP_001372217.1:p.Leu790=
NM_001385290.1:c.2377T>C	NP_001372219.1:p.Leu793=
NM_001385292.1:c.2365T>C	NP_001372221.1:p.Leu789=