Canonical Allele Identifier: CA1881266296

Gene: HMCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433418C= , CM000671.2:g.130433418C=	GRCh38
NC_000009.11:g.133308805C= , CM000671.1:g.133308805C=	GRCh37
NC_000009.10:g.132298626C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14908C=	ENSP00000485357.2:p.Pro4970=
ENST00000683500.2:c.14965C= MANE Select	ENSP00000508292.2:p.Pro4989=
ENST00000623487.1:n.3311C=
ENST00000624552.3:c.14905C=	ENSP00000485357.1:p.Pro4969=
NM_001291815.1:c.14965C=	NP_001278744.1:p.Pro4989=
XM_011518465.1:c.14842C=	XP_011516767.1:p.Pro4948=
XM_011518466.1:c.14833C=	XP_011516768.1:p.Pro4945=
XM_011518467.1:c.14788C=	XP_011516769.1:p.Pro4930=
NM_001291815.2:c.14965C= MANE Select	NP_001278744.1:p.Pro4989=
XM_011518465.2:c.14842C=	XP_011516767.1:p.Pro4948=
XM_011518466.2:c.14833C=	XP_011516768.1:p.Pro4945=
XM_011518467.2:c.14788C=	XP_011516769.1:p.Pro4930=
XM_017014585.1:c.11746C=	XP_016870074.1:p.Pro3916=
XM_017014586.1:c.7543C=	XP_016870075.1:p.Pro2515=
XR_001746957.1:n.92+203G=
XR_001746958.1:n.92+203G=