Canonical Allele Identifier: CA1881266158

Gene: HMCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433362G= , CM000671.2:g.130433362G=	GRCh38
NC_000009.11:g.133308749G= , CM000671.1:g.133308749G=	GRCh37
NC_000009.10:g.132298570G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14852G=	ENSP00000485357.2:p.Arg4951=
ENST00000683500.2:c.14909G= MANE Select	ENSP00000508292.2:p.Arg4970=
ENST00000623487.1:n.3255G=
ENST00000624552.3:c.14849G=	ENSP00000485357.1:p.Arg4950=
NM_001291815.1:c.14909G=	NP_001278744.1:p.Arg4970=
XM_011518465.1:c.14786G=	XP_011516767.1:p.Arg4929=
XM_011518466.1:c.14777G=	XP_011516768.1:p.Arg4926=
XM_011518467.1:c.14732G=	XP_011516769.1:p.Arg4911=
NM_001291815.2:c.14909G= MANE Select	NP_001278744.1:p.Arg4970=
XM_011518465.2:c.14786G=	XP_011516767.1:p.Arg4929=
XM_011518466.2:c.14777G=	XP_011516768.1:p.Arg4926=
XM_011518467.2:c.14732G=	XP_011516769.1:p.Arg4911=
XM_017014585.1:c.11690G=	XP_016870074.1:p.Arg3897=
XM_017014586.1:c.7487G=	XP_016870075.1:p.Arg2496=
XR_001746957.1:n.92+259C=
XR_001746958.1:n.92+259C=