Canonical Allele Identifier: CA1881266273

Gene: HMCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433410G= , CM000671.2:g.130433410G=	GRCh38
NC_000009.11:g.133308797G= , CM000671.1:g.133308797G=	GRCh37
NC_000009.10:g.132298618G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14900G=	ENSP00000485357.2:p.Arg4967=
ENST00000683500.2:c.14957G= MANE Select	ENSP00000508292.2:p.Arg4986=
ENST00000623487.1:n.3303G=
ENST00000624552.3:c.14897G=	ENSP00000485357.1:p.Arg4966=
NM_001291815.1:c.14957G=	NP_001278744.1:p.Arg4986=
XM_011518465.1:c.14834G=	XP_011516767.1:p.Arg4945=
XM_011518466.1:c.14825G=	XP_011516768.1:p.Arg4942=
XM_011518467.1:c.14780G=	XP_011516769.1:p.Arg4927=
NM_001291815.2:c.14957G= MANE Select	NP_001278744.1:p.Arg4986=
XM_011518465.2:c.14834G=	XP_011516767.1:p.Arg4945=
XM_011518466.2:c.14825G=	XP_011516768.1:p.Arg4942=
XM_011518467.2:c.14780G=	XP_011516769.1:p.Arg4927=
XM_017014585.1:c.11738G=	XP_016870074.1:p.Arg3913=
XM_017014586.1:c.7535G=	XP_016870075.1:p.Arg2512=
XR_001746957.1:n.92+211C=
XR_001746958.1:n.92+211C=