Canonical Allele Identifier: CA1881266226

Gene: HMCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433391C= , CM000671.2:g.130433391C=	GRCh38
NC_000009.11:g.133308778C= , CM000671.1:g.133308778C=	GRCh37
NC_000009.10:g.132298599C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14881C=	ENSP00000485357.2:p.Pro4961=
ENST00000683500.2:c.14938C= MANE Select	ENSP00000508292.2:p.Pro4980=
ENST00000623487.1:n.3284C=
ENST00000624552.3:c.14878C=	ENSP00000485357.1:p.Pro4960=
NM_001291815.1:c.14938C=	NP_001278744.1:p.Pro4980=
XM_011518465.1:c.14815C=	XP_011516767.1:p.Pro4939=
XM_011518466.1:c.14806C=	XP_011516768.1:p.Pro4936=
XM_011518467.1:c.14761C=	XP_011516769.1:p.Pro4921=
NM_001291815.2:c.14938C= MANE Select	NP_001278744.1:p.Pro4980=
XM_011518465.2:c.14815C=	XP_011516767.1:p.Pro4939=
XM_011518466.2:c.14806C=	XP_011516768.1:p.Pro4936=
XM_011518467.2:c.14761C=	XP_011516769.1:p.Pro4921=
XM_017014585.1:c.11719C=	XP_016870074.1:p.Pro3907=
XM_017014586.1:c.7516C=	XP_016870075.1:p.Pro2506=
XR_001746957.1:n.92+230G=
XR_001746958.1:n.92+230G=