Canonical Allele Identifier: CA1881266191

Gene: HMCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433375C= , CM000671.2:g.130433375C=	GRCh38
NC_000009.11:g.133308762C= , CM000671.1:g.133308762C=	GRCh37
NC_000009.10:g.132298583C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14865C=	ENSP00000485357.2:p.Asp4955=
ENST00000683500.2:c.14922C= MANE Select	ENSP00000508292.2:p.Asp4974=
ENST00000623487.1:n.3268C=
ENST00000624552.3:c.14862C=	ENSP00000485357.1:p.Asp4954=
NM_001291815.1:c.14922C=	NP_001278744.1:p.Asp4974=
XM_011518465.1:c.14799C=	XP_011516767.1:p.Asp4933=
XM_011518466.1:c.14790C=	XP_011516768.1:p.Asp4930=
XM_011518467.1:c.14745C=	XP_011516769.1:p.Asp4915=
NM_001291815.2:c.14922C= MANE Select	NP_001278744.1:p.Asp4974=
XM_011518465.2:c.14799C=	XP_011516767.1:p.Asp4933=
XM_011518466.2:c.14790C=	XP_011516768.1:p.Asp4930=
XM_011518467.2:c.14745C=	XP_011516769.1:p.Asp4915=
XM_017014585.1:c.11703C=	XP_016870074.1:p.Asp3901=
XM_017014586.1:c.7500C=	XP_016870075.1:p.Asp2500=
XR_001746957.1:n.92+246G=
XR_001746958.1:n.92+246G=