Canonical Allele Identifier: CA1881266137

Gene: HMCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433350C= , CM000671.2:g.130433350C=	GRCh38
NC_000009.11:g.133308737C= , CM000671.1:g.133308737C=	GRCh37
NC_000009.10:g.132298558C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14840C=	ENSP00000485357.2:p.Thr4947=
ENST00000683500.2:c.14897C= MANE Select	ENSP00000508292.2:p.Thr4966=
ENST00000623487.1:n.3243C=
ENST00000624552.3:c.14837C=	ENSP00000485357.1:p.Thr4946=
NM_001291815.1:c.14897C=	NP_001278744.1:p.Thr4966=
XM_011518465.1:c.14774C=	XP_011516767.1:p.Thr4925=
XM_011518466.1:c.14765C=	XP_011516768.1:p.Thr4922=
XM_011518467.1:c.14720C=	XP_011516769.1:p.Thr4907=
NM_001291815.2:c.14897C= MANE Select	NP_001278744.1:p.Thr4966=
XM_011518465.2:c.14774C=	XP_011516767.1:p.Thr4925=
XM_011518466.2:c.14765C=	XP_011516768.1:p.Thr4922=
XM_011518467.2:c.14720C=	XP_011516769.1:p.Thr4907=
XM_017014585.1:c.11678C=	XP_016870074.1:p.Thr3893=
XM_017014586.1:c.7475C=	XP_016870075.1:p.Thr2492=
XR_001746957.1:n.92+271G=
XR_001746958.1:n.92+271G=