Canonical Allele Identifier: CA1881266217

Gene: HMCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433388G= , CM000671.2:g.130433388G=	GRCh38
NC_000009.11:g.133308775G= , CM000671.1:g.133308775G=	GRCh37
NC_000009.10:g.132298596G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14878G=	ENSP00000485357.2:p.Gly4960=
ENST00000683500.2:c.14935G= MANE Select	ENSP00000508292.2:p.Gly4979=
ENST00000623487.1:n.3281G=
ENST00000624552.3:c.14875G=	ENSP00000485357.1:p.Gly4959=
NM_001291815.1:c.14935G=	NP_001278744.1:p.Gly4979=
XM_011518465.1:c.14812G=	XP_011516767.1:p.Gly4938=
XM_011518466.1:c.14803G=	XP_011516768.1:p.Gly4935=
XM_011518467.1:c.14758G=	XP_011516769.1:p.Gly4920=
NM_001291815.2:c.14935G= MANE Select	NP_001278744.1:p.Gly4979=
XM_011518465.2:c.14812G=	XP_011516767.1:p.Gly4938=
XM_011518466.2:c.14803G=	XP_011516768.1:p.Gly4935=
XM_011518467.2:c.14758G=	XP_011516769.1:p.Gly4920=
XM_017014585.1:c.11716G=	XP_016870074.1:p.Gly3906=
XM_017014586.1:c.7513G=	XP_016870075.1:p.Gly2505=
XR_001746957.1:n.92+233C=
XR_001746958.1:n.92+233C=