Canonical Allele Identifier: CA1881266257

Gene: HMCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433402G= , CM000671.2:g.130433402G=	GRCh38
NC_000009.11:g.133308789G= , CM000671.1:g.133308789G=	GRCh37
NC_000009.10:g.132298610G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000624552.4:c.14892G=	ENSP00000485357.2:p.Leu4964=
ENST00000683500.2:c.14949G= MANE Select	ENSP00000508292.2:p.Leu4983=
ENST00000623487.1:n.3295G=
ENST00000624552.3:c.14889G=	ENSP00000485357.1:p.Leu4963=
NM_001291815.1:c.14949G=	NP_001278744.1:p.Leu4983=
XM_011518465.1:c.14826G=	XP_011516767.1:p.Leu4942=
XM_011518466.1:c.14817G=	XP_011516768.1:p.Leu4939=
XM_011518467.1:c.14772G=	XP_011516769.1:p.Leu4924=
NM_001291815.2:c.14949G= MANE Select	NP_001278744.1:p.Leu4983=
XM_011518465.2:c.14826G=	XP_011516767.1:p.Leu4942=
XM_011518466.2:c.14817G=	XP_011516768.1:p.Leu4939=
XM_011518467.2:c.14772G=	XP_011516769.1:p.Leu4924=
XM_017014585.1:c.11730G=	XP_016870074.1:p.Leu3910=
XM_017014586.1:c.7527G=	XP_016870075.1:p.Leu2509=
XR_001746957.1:n.92+219C=
XR_001746958.1:n.92+219C=