Canonical Allele Identifier: CA1881266433

Gene: HMCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433481G= , CM000671.2:g.130433481G=	GRCh38
NC_000009.11:g.133308868G= , CM000671.1:g.133308868G=	GRCh37
NC_000009.10:g.132298689G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14971G=	ENSP00000485357.2:p.Gly4991=
ENST00000683500.2:c.15028G= MANE Select	ENSP00000508292.2:p.Gly5010=
ENST00000623487.1:n.3374G=
ENST00000624552.3:c.14968G=	ENSP00000485357.1:p.Gly4990=
NM_001291815.1:c.15028G=	NP_001278744.1:p.Gly5010=
XM_011518465.1:c.14905G=	XP_011516767.1:p.Gly4969=
XM_011518466.1:c.14896G=	XP_011516768.1:p.Gly4966=
XM_011518467.1:c.14851G=	XP_011516769.1:p.Gly4951=
NM_001291815.2:c.15028G= MANE Select	NP_001278744.1:p.Gly5010=
XM_011518465.2:c.14905G=	XP_011516767.1:p.Gly4969=
XM_011518466.2:c.14896G=	XP_011516768.1:p.Gly4966=
XM_011518467.2:c.14851G=	XP_011516769.1:p.Gly4951=
XM_017014585.1:c.11809G=	XP_016870074.1:p.Gly3937=
XM_017014586.1:c.7606G=	XP_016870075.1:p.Gly2536=
XR_001746957.1:n.92+140C=
XR_001746958.1:n.92+140C=