Canonical Allele Identifier: CA2547772721

Gene: KIT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54727966_54727967insG , CM000666.2:g.54727966_54727967insG	GRCh38
NC_000004.11:g.55594132_55594133insG , CM000666.1:g.55594132_55594133insG	GRCh37
NC_000004.10:g.55288889_55288890insG	NCBI36
NG_007456.1:g.74972_74973insG , LRG_307:g.74972_74973insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412167.7:c.1870+39_1870+40insG	ENSP00000390987.3:n.1870+39_1870+40insG
ENST00000685269.1:n.1957+39_1957+40insG
ENST00000686011.1:c.1867+39_1867+40insG	ENSP00000509704.1:n.1867+39_1867+40insG
ENST00000687109.1:c.1882+39_1882+40insG	ENSP00000509371.1:n.1882+39_1882+40insG
ENST00000687208.1:n.2294+39_2294+40insG
ENST00000687246.1:c.1867+39_1867+40insG	ENSP00000509114.1:n.1867+39_1867+40insG
ENST00000687265.1:n.2037+39_2037+40insG
ENST00000687295.1:c.1867+39_1867+40insG	ENSP00000509450.1:n.1867+39_1867+40insG
ENST00000689832.1:c.1882+39_1882+40insG	ENSP00000509084.1:n.1882+39_1882+40insG
ENST00000689994.1:c.1369+39_1369+40insG	ENSP00000509156.1:n.1369+39_1369+40insG
ENST00000690543.1:c.1870+39_1870+40insG	ENSP00000508831.1:n.1870+39_1870+40insG
ENST00000690917.1:n.2097+39_2097+40insG
ENST00000691361.1:n.789+39_789+40insG
ENST00000692783.1:c.1879+39_1879+40insG	ENSP00000508733.1:n.1879+39_1879+40insG
ENST00000692991.1:n.1976+39_1976+40insG
ENST00000288135.6:c.1879+39_1879+40insG MANE Select	ENSP00000288135.6:n.1879+39_1879+40insG
ENST00000288135.5:c.1879+39_1879+40insG	ENSP00000288135.5:n.1879+39_1879+40insG
ENST00000412167.6:c.1867+39_1867+40insG	ENSP00000390987.2:n.1867+39_1867+40insG
NM_000222.2:c.1879+39_1879+40insG , LRG_307t1:c.1879+39_1879+40insG	NP_000213.1:n.1879+39_1879+40insG
NM_001093772.1:c.1867+39_1867+40insG	NP_001087241.1:n.1867+39_1867+40insG
XM_005265740.1:c.1882+39_1882+40insG	XP_005265797.1:n.1882+39_1882+40insG
XM_005265741.1:c.1882+39_1882+40insG	XP_005265798.1:n.1882+39_1882+40insG
XM_005265742.1:c.1870+39_1870+40insG	XP_005265799.1:n.1870+39_1870+40insG
XM_005265742.3:c.1870+39_1870+40insG	XP_005265799.1:n.1870+39_1870+40insG
XM_017008178.1:c.1879+39_1879+40insG	XP_016863667.1:n.1879+39_1879+40insG
XM_017008179.1:c.1870+39_1870+40insG	XP_016863668.1:n.1870+39_1870+40insG
XM_017008180.1:c.1867+39_1867+40insG	XP_016863669.1:n.1867+39_1867+40insG
NM_000222.3:c.1879+39_1879+40insG MANE Select	NP_000213.1:n.1879+39_1879+40insG
NM_001093772.2:c.1867+39_1867+40insG	NP_001087241.1:n.1867+39_1867+40insG
NM_001385284.1:c.1882+39_1882+40insG	NP_001372213.1:n.1882+39_1882+40insG
NM_001385285.1:c.1879+39_1879+40insG	NP_001372214.1:n.1879+39_1879+40insG
NM_001385286.1:c.1867+39_1867+40insG	NP_001372215.1:n.1867+39_1867+40insG
NM_001385288.1:c.1870+39_1870+40insG	NP_001372217.1:n.1870+39_1870+40insG
NM_001385290.1:c.1882+39_1882+40insG	NP_001372219.1:n.1882+39_1882+40insG
NM_001385292.1:c.1870+39_1870+40insG	NP_001372221.1:n.1870+39_1870+40insG