Canonical Allele Identifier: CA1881266155

Gene: HMCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433360G= , CM000671.2:g.130433360G=	GRCh38
NC_000009.11:g.133308747G= , CM000671.1:g.133308747G=	GRCh37
NC_000009.10:g.132298568G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14850G=	ENSP00000485357.2:p.Arg4950=
ENST00000683500.2:c.14907G= MANE Select	ENSP00000508292.2:p.Arg4969=
ENST00000623487.1:n.3253G=
ENST00000624552.3:c.14847G=	ENSP00000485357.1:p.Arg4949=
NM_001291815.1:c.14907G=	NP_001278744.1:p.Arg4969=
XM_011518465.1:c.14784G=	XP_011516767.1:p.Arg4928=
XM_011518466.1:c.14775G=	XP_011516768.1:p.Arg4925=
XM_011518467.1:c.14730G=	XP_011516769.1:p.Arg4910=
NM_001291815.2:c.14907G= MANE Select	NP_001278744.1:p.Arg4969=
XM_011518465.2:c.14784G=	XP_011516767.1:p.Arg4928=
XM_011518466.2:c.14775G=	XP_011516768.1:p.Arg4925=
XM_011518467.2:c.14730G=	XP_011516769.1:p.Arg4910=
XM_017014585.1:c.11688G=	XP_016870074.1:p.Arg3896=
XM_017014586.1:c.7485G=	XP_016870075.1:p.Arg2495=
XR_001746957.1:n.92+261C=
XR_001746958.1:n.92+261C=