Canonical Allele Identifier: CA915943134

Gene: KIT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54658088C>G , CM000666.2:g.54658088C>G	GRCh38
NC_000004.11:g.55524255C>G , CM000666.1:g.55524255C>G	GRCh37
NC_000004.10:g.55219012C>G	NCBI36
NG_007456.1:g.5095C>G , LRG_307:g.5095C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.67+7C>G	ENSP00000390987.3:n.67+7C>G
ENST00000686011.1:c.67+7C>G	ENSP00000509704.1:n.67+7C>G
ENST00000687109.1:c.67+7C>G	ENSP00000509371.1:n.67+7C>G
ENST00000687246.1:c.67+7C>G	ENSP00000509114.1:n.67+7C>G
ENST00000687295.1:c.67+7C>G	ENSP00000509450.1:n.67+7C>G
ENST00000689832.1:c.67+7C>G	ENSP00000509084.1:n.67+7C>G
ENST00000689994.1:c.-444+733C>G	ENSP00000509156.1:n.-444+733C>G
ENST00000690519.1:c.67+7C>G	ENSP00000508845.1:n.67+7C>G
ENST00000690543.1:c.67+7C>G	ENSP00000508831.1:n.67+7C>G
ENST00000692783.1:c.67+7C>G	ENSP00000508733.1:n.67+7C>G
ENST00000288135.6:c.67+7C>G MANE Select	ENSP00000288135.6:n.67+7C>G
ENST00000288135.5:c.67+7C>G	ENSP00000288135.5:n.67+7C>G
ENST00000412167.6:c.67+7C>G	ENSP00000390987.2:n.67+7C>G
ENST00000514582.1:n.143+7C>G
NM_000222.2:c.67+7C>G , LRG_307t1:c.67+7C>G	NP_000213.1:n.67+7C>G
NM_001093772.1:c.67+7C>G	NP_001087241.1:n.67+7C>G
XM_005265740.1:c.67+7C>G	XP_005265797.1:n.67+7C>G
XM_005265741.1:c.67+7C>G	XP_005265798.1:n.67+7C>G
XM_005265742.1:c.67+7C>G	XP_005265799.1:n.67+7C>G
XM_005265742.3:c.67+7C>G	XP_005265799.1:n.67+7C>G
XM_017008178.1:c.67+7C>G	XP_016863667.1:n.67+7C>G
XM_017008179.1:c.67+7C>G	XP_016863668.1:n.67+7C>G
XM_017008180.1:c.67+7C>G	XP_016863669.1:n.67+7C>G
NM_000222.3:c.67+7C>G MANE Select	NP_000213.1:n.67+7C>G
NM_001093772.2:c.67+7C>G	NP_001087241.1:n.67+7C>G
NM_001385284.1:c.67+7C>G	NP_001372213.1:n.67+7C>G
NM_001385285.1:c.67+7C>G	NP_001372214.1:n.67+7C>G
NM_001385286.1:c.67+7C>G	NP_001372215.1:n.67+7C>G
NM_001385288.1:c.67+7C>G	NP_001372217.1:n.67+7C>G
NM_001385290.1:c.67+7C>G	NP_001372219.1:n.67+7C>G
NM_001385292.1:c.67+7C>G	NP_001372221.1:n.67+7C>G