Canonical Allele Identifier: CA356911348

Gene: KIT

Linked Data

• MyVariant Identifiers: chr4:g.55599239A>G (hg19) ; chr4:g.54733073A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54733073A>G , CM000666.2:g.54733073A>G	GRCh38
NC_000004.11:g.55599239A>G , CM000666.1:g.55599239A>G	GRCh37
NC_000004.10:g.55293996A>G	NCBI36
NG_007456.1:g.80079A>G , LRG_307:g.80079A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000412167.7:c.2353A>G	ENSP00000390987.3:p.Ile785Val
ENST00000685269.1:n.2443A>G
ENST00000686011.1:c.2350A>G	ENSP00000509704.1:p.Ile784Val
ENST00000687109.1:c.2368A>G	ENSP00000509371.1:p.Ile790Val
ENST00000687208.1:n.2777A>G
ENST00000687246.1:c.2349+1075A>G	ENSP00000509114.1:n.2349+1075A>G
ENST00000687265.1:n.2523A>G
ENST00000687295.1:c.2353A>G	ENSP00000509450.1:p.Ile785Val
ENST00000688060.1:n.162A>G
ENST00000688704.1:n.1377A>G
ENST00000689832.1:c.2365A>G	ENSP00000509084.1:p.Ile789Val
ENST00000689994.1:c.1855A>G	ENSP00000509156.1:p.Ile619Val
ENST00000690543.1:c.2356A>G	ENSP00000508831.1:p.Ile786Val
ENST00000690917.1:n.2583A>G
ENST00000691361.1:n.1275A>G
ENST00000692783.1:c.2362A>G	ENSP00000508733.1:p.Ile788Val
ENST00000692991.1:n.2462A>G
ENST00000288135.6:c.2365A>G MANE Select	ENSP00000288135.6:p.Ile789Val
ENST00000288135.5:c.2365A>G	ENSP00000288135.5:p.Ile789Val
ENST00000412167.6:c.2353A>G	ENSP00000390987.2:p.Ile785Val
ENST00000512959.1:n.418A>G
NM_000222.2:c.2365A>G , LRG_307t1:c.2365A>G	NP_000213.1:p.Ile789Val
NM_001093772.1:c.2353A>G	NP_001087241.1:p.Ile785Val
XM_005265740.1:c.2368A>G	XP_005265797.1:p.Ile790Val
XM_005265741.1:c.2365A>G	XP_005265798.1:p.Ile789Val
XM_005265742.1:c.2356A>G	XP_005265799.1:p.Ile786Val
XM_005265742.3:c.2356A>G	XP_005265799.1:p.Ile786Val
XM_017008178.1:c.2362A>G	XP_016863667.1:p.Ile788Val
XM_017008179.1:c.2353A>G	XP_016863668.1:p.Ile785Val
XM_017008180.1:c.2350A>G	XP_016863669.1:p.Ile784Val
NM_000222.3:c.2365A>G MANE Select	NP_000213.1:p.Ile789Val
NM_001093772.2:c.2353A>G	NP_001087241.1:p.Ile785Val
NM_001385284.1:c.2368A>G	NP_001372213.1:p.Ile790Val
NM_001385285.1:c.2362A>G	NP_001372214.1:p.Ile788Val
NM_001385286.1:c.2350A>G	NP_001372215.1:p.Ile784Val
NM_001385288.1:c.2356A>G	NP_001372217.1:p.Ile786Val
NM_001385290.1:c.2365A>G	NP_001372219.1:p.Ile789Val
NM_001385292.1:c.2353A>G	NP_001372221.1:p.Ile785Val