Canonical Allele Identifier: CA1881266361

Gene: HMCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433448G= , CM000671.2:g.130433448G=	GRCh38
NC_000009.11:g.133308835G= , CM000671.1:g.133308835G=	GRCh37
NC_000009.10:g.132298656G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14938G=	ENSP00000485357.2:p.Asp4980=
ENST00000683500.2:c.14995G= MANE Select	ENSP00000508292.2:p.Asp4999=
ENST00000623487.1:n.3341G=
ENST00000624552.3:c.14935G=	ENSP00000485357.1:p.Asp4979=
NM_001291815.1:c.14995G=	NP_001278744.1:p.Asp4999=
XM_011518465.1:c.14872G=	XP_011516767.1:p.Asp4958=
XM_011518466.1:c.14863G=	XP_011516768.1:p.Asp4955=
XM_011518467.1:c.14818G=	XP_011516769.1:p.Asp4940=
NM_001291815.2:c.14995G= MANE Select	NP_001278744.1:p.Asp4999=
XM_011518465.2:c.14872G=	XP_011516767.1:p.Asp4958=
XM_011518466.2:c.14863G=	XP_011516768.1:p.Asp4955=
XM_011518467.2:c.14818G=	XP_011516769.1:p.Asp4940=
XM_017014585.1:c.11776G=	XP_016870074.1:p.Asp3926=
XM_017014586.1:c.7573G=	XP_016870075.1:p.Asp2525=
XR_001746957.1:n.92+173C=
XR_001746958.1:n.92+173C=