Canonical Allele Identifier: CA1881266279

Gene: HMCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433412C= , CM000671.2:g.130433412C=	GRCh38
NC_000009.11:g.133308799C= , CM000671.1:g.133308799C=	GRCh37
NC_000009.10:g.132298620C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14902C=	ENSP00000485357.2:p.Leu4968=
ENST00000683500.2:c.14959C= MANE Select	ENSP00000508292.2:p.Leu4987=
ENST00000623487.1:n.3305C=
ENST00000624552.3:c.14899C=	ENSP00000485357.1:p.Leu4967=
NM_001291815.1:c.14959C=	NP_001278744.1:p.Leu4987=
XM_011518465.1:c.14836C=	XP_011516767.1:p.Leu4946=
XM_011518466.1:c.14827C=	XP_011516768.1:p.Leu4943=
XM_011518467.1:c.14782C=	XP_011516769.1:p.Leu4928=
NM_001291815.2:c.14959C= MANE Select	NP_001278744.1:p.Leu4987=
XM_011518465.2:c.14836C=	XP_011516767.1:p.Leu4946=
XM_011518466.2:c.14827C=	XP_011516768.1:p.Leu4943=
XM_011518467.2:c.14782C=	XP_011516769.1:p.Leu4928=
XM_017014585.1:c.11740C=	XP_016870074.1:p.Leu3914=
XM_017014586.1:c.7537C=	XP_016870075.1:p.Leu2513=
XR_001746957.1:n.92+209G=
XR_001746958.1:n.92+209G=