Canonical Allele Identifier: CA1881266381

Gene: HMCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433457C= , CM000671.2:g.130433457C=	GRCh38
NC_000009.11:g.133308844C= , CM000671.1:g.133308844C=	GRCh37
NC_000009.10:g.132298665C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14947C=	ENSP00000485357.2:p.Arg4983=
ENST00000683500.2:c.15004C= MANE Select	ENSP00000508292.2:p.Arg5002=
ENST00000623487.1:n.3350C=
ENST00000624552.3:c.14944C=	ENSP00000485357.1:p.Arg4982=
NM_001291815.1:c.15004C=	NP_001278744.1:p.Arg5002=
XM_011518465.1:c.14881C=	XP_011516767.1:p.Arg4961=
XM_011518466.1:c.14872C=	XP_011516768.1:p.Arg4958=
XM_011518467.1:c.14827C=	XP_011516769.1:p.Arg4943=
NM_001291815.2:c.15004C= MANE Select	NP_001278744.1:p.Arg5002=
XM_011518465.2:c.14881C=	XP_011516767.1:p.Arg4961=
XM_011518466.2:c.14872C=	XP_011516768.1:p.Arg4958=
XM_011518467.2:c.14827C=	XP_011516769.1:p.Arg4943=
XM_017014585.1:c.11785C=	XP_016870074.1:p.Arg3929=
XM_017014586.1:c.7582C=	XP_016870075.1:p.Arg2528=
XR_001746957.1:n.92+164G=
XR_001746958.1:n.92+164G=