Canonical Allele Identifier: CA356897847

Gene: KIT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54658024G>T , CM000666.2:g.54658024G>T	GRCh38
NC_000004.11:g.55524191G>T , CM000666.1:g.55524191G>T	GRCh37
NC_000004.10:g.55218948G>T	NCBI36
NG_007456.1:g.5031G>T , LRG_307:g.5031G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.10G>T	ENSP00000390987.3:p.Ala4Ser
ENST00000686011.1:c.10G>T	ENSP00000509704.1:p.Ala4Ser
ENST00000687109.1:c.10G>T	ENSP00000509371.1:p.Ala4Ser
ENST00000687246.1:c.10G>T	ENSP00000509114.1:p.Ala4Ser
ENST00000687295.1:c.10G>T	ENSP00000509450.1:p.Ala4Ser
ENST00000689832.1:c.10G>T	ENSP00000509084.1:p.Ala4Ser
ENST00000689994.1:c.-444+669G>T	ENSP00000509156.1:n.-444+669G>T
ENST00000690519.1:c.10G>T	ENSP00000508845.1:p.Ala4Ser
ENST00000690543.1:c.10G>T	ENSP00000508831.1:p.Ala4Ser
ENST00000692783.1:c.10G>T	ENSP00000508733.1:p.Ala4Ser
ENST00000288135.6:c.10G>T MANE Select	ENSP00000288135.6:p.Ala4Ser
ENST00000288135.5:c.10G>T	ENSP00000288135.5:p.Ala4Ser
ENST00000412167.6:c.10G>T	ENSP00000390987.2:p.Ala4Ser
ENST00000514582.1:n.86G>T
NM_000222.2:c.10G>T , LRG_307t1:c.10G>T	NP_000213.1:p.Ala4Ser
NM_001093772.1:c.10G>T	NP_001087241.1:p.Ala4Ser
XM_005265740.1:c.10G>T	XP_005265797.1:p.Ala4Ser
XM_005265741.1:c.10G>T	XP_005265798.1:p.Ala4Ser
XM_005265742.1:c.10G>T	XP_005265799.1:p.Ala4Ser
XM_005265742.3:c.10G>T	XP_005265799.1:p.Ala4Ser
XM_017008178.1:c.10G>T	XP_016863667.1:p.Ala4Ser
XM_017008179.1:c.10G>T	XP_016863668.1:p.Ala4Ser
XM_017008180.1:c.10G>T	XP_016863669.1:p.Ala4Ser
NM_000222.3:c.10G>T MANE Select	NP_000213.1:p.Ala4Ser
NM_001093772.2:c.10G>T	NP_001087241.1:p.Ala4Ser
NM_001385284.1:c.10G>T	NP_001372213.1:p.Ala4Ser
NM_001385285.1:c.10G>T	NP_001372214.1:p.Ala4Ser
NM_001385286.1:c.10G>T	NP_001372215.1:p.Ala4Ser
NM_001385288.1:c.10G>T	NP_001372217.1:p.Ala4Ser
NM_001385290.1:c.10G>T	NP_001372219.1:p.Ala4Ser
NM_001385292.1:c.10G>T	NP_001372221.1:p.Ala4Ser