Canonical Allele Identifier: CA2066353250

Gene: VSIG10

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.118086590A= , CM000674.2:g.118086590A=	GRCh38
NC_000012.11:g.118524395A= , CM000674.1:g.118524395A=	GRCh37
NC_000012.10:g.117008778A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359236.10:c.362-4161T= MANE Select	ENSP00000352172.5:n.362-4161T=
ENST00000359236.9:c.362-4161T=	ENSP00000352172.5:n.362-4161T=
ENST00000536905.5:n.873-4161T=
ENST00000538357.1:c.362-6984T=	ENSP00000442861.1:n.362-6984T=
NM_019086.5:c.362-4161T=	NP_061959.2:n.362-4161T=
XM_006719467.2:c.362-6984T=	XP_006719530.1:n.362-6984T=
XM_011538502.1:c.362-4161T=	XP_011536804.1:n.362-4161T=
XR_944592.1:n.696-4161T=
XR_944593.1:n.696-4161T=
XR_944594.1:n.696-4161T=
XM_005253908.4:c.-130-4161T=	XP_005253965.1:n.-130-4161T=
XM_017019504.1:c.-130-4161T=	XP_016874993.1:n.-130-4161T=
XM_017019505.1:c.-130-4161T=	XP_016874994.1:n.-130-4161T=
XM_017019506.1:c.-338-4161T=	XP_016874995.1:n.-338-4161T=
XR_002957341.1:n.696-4161T=
XR_002957342.1:n.696-4161T=
XR_002957343.1:n.696-4161T=
NM_019086.6:c.362-4161T= MANE Select	NP_061959.2:n.362-4161T=