Canonical Allele Identifier: CA1881266183

Gene: HMCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433370C= , CM000671.2:g.130433370C=	GRCh38
NC_000009.11:g.133308757C= , CM000671.1:g.133308757C=	GRCh37
NC_000009.10:g.132298578C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14860C=	ENSP00000485357.2:p.Gln4954=
ENST00000683500.2:c.14917C= MANE Select	ENSP00000508292.2:p.Gln4973=
ENST00000623487.1:n.3263C=
ENST00000624552.3:c.14857C=	ENSP00000485357.1:p.Gln4953=
NM_001291815.1:c.14917C=	NP_001278744.1:p.Gln4973=
XM_011518465.1:c.14794C=	XP_011516767.1:p.Gln4932=
XM_011518466.1:c.14785C=	XP_011516768.1:p.Gln4929=
XM_011518467.1:c.14740C=	XP_011516769.1:p.Gln4914=
NM_001291815.2:c.14917C= MANE Select	NP_001278744.1:p.Gln4973=
XM_011518465.2:c.14794C=	XP_011516767.1:p.Gln4932=
XM_011518466.2:c.14785C=	XP_011516768.1:p.Gln4929=
XM_011518467.2:c.14740C=	XP_011516769.1:p.Gln4914=
XM_017014585.1:c.11698C=	XP_016870074.1:p.Gln3900=
XM_017014586.1:c.7495C=	XP_016870075.1:p.Gln2499=
XR_001746957.1:n.92+251G=
XR_001746958.1:n.92+251G=