Canonical Allele Identifier: CA1881266269

Gene: HMCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433408C= , CM000671.2:g.130433408C=	GRCh38
NC_000009.11:g.133308795C= , CM000671.1:g.133308795C=	GRCh37
NC_000009.10:g.132298616C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14898C=	ENSP00000485357.2:p.Tyr4966=
ENST00000683500.2:c.14955C= MANE Select	ENSP00000508292.2:p.Tyr4985=
ENST00000623487.1:n.3301C=
ENST00000624552.3:c.14895C=	ENSP00000485357.1:p.Tyr4965=
NM_001291815.1:c.14955C=	NP_001278744.1:p.Tyr4985=
XM_011518465.1:c.14832C=	XP_011516767.1:p.Tyr4944=
XM_011518466.1:c.14823C=	XP_011516768.1:p.Tyr4941=
XM_011518467.1:c.14778C=	XP_011516769.1:p.Tyr4926=
NM_001291815.2:c.14955C= MANE Select	NP_001278744.1:p.Tyr4985=
XM_011518465.2:c.14832C=	XP_011516767.1:p.Tyr4944=
XM_011518466.2:c.14823C=	XP_011516768.1:p.Tyr4941=
XM_011518467.2:c.14778C=	XP_011516769.1:p.Tyr4926=
XM_017014585.1:c.11736C=	XP_016870074.1:p.Tyr3912=
XM_017014586.1:c.7533C=	XP_016870075.1:p.Tyr2511=
XR_001746957.1:n.92+213G=
XR_001746958.1:n.92+213G=