Canonical Allele Identifier: CA1881266426

Gene: HMCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433475G= , CM000671.2:g.130433475G=	GRCh38
NC_000009.11:g.133308862G= , CM000671.1:g.133308862G=	GRCh37
NC_000009.10:g.132298683G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14965G=	ENSP00000485357.2:p.Glu4989=
ENST00000683500.2:c.15022G= MANE Select	ENSP00000508292.2:p.Glu5008=
ENST00000623487.1:n.3368G=
ENST00000624552.3:c.14962G=	ENSP00000485357.1:p.Glu4988=
NM_001291815.1:c.15022G=	NP_001278744.1:p.Glu5008=
XM_011518465.1:c.14899G=	XP_011516767.1:p.Glu4967=
XM_011518466.1:c.14890G=	XP_011516768.1:p.Glu4964=
XM_011518467.1:c.14845G=	XP_011516769.1:p.Glu4949=
NM_001291815.2:c.15022G= MANE Select	NP_001278744.1:p.Glu5008=
XM_011518465.2:c.14899G=	XP_011516767.1:p.Glu4967=
XM_011518466.2:c.14890G=	XP_011516768.1:p.Glu4964=
XM_011518467.2:c.14845G=	XP_011516769.1:p.Glu4949=
XM_017014585.1:c.11803G=	XP_016870074.1:p.Glu3935=
XM_017014586.1:c.7600G=	XP_016870075.1:p.Glu2534=
XR_001746957.1:n.92+146C=
XR_001746958.1:n.92+146C=