Canonical Allele Identifier: CA1881266145

Gene: HMCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433357C= , CM000671.2:g.130433357C=	GRCh38
NC_000009.11:g.133308744C= , CM000671.1:g.133308744C=	GRCh37
NC_000009.10:g.132298565C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14847C=	ENSP00000485357.2:p.Phe4949=
ENST00000683500.2:c.14904C= MANE Select	ENSP00000508292.2:p.Phe4968=
ENST00000623487.1:n.3250C=
ENST00000624552.3:c.14844C=	ENSP00000485357.1:p.Phe4948=
NM_001291815.1:c.14904C=	NP_001278744.1:p.Phe4968=
XM_011518465.1:c.14781C=	XP_011516767.1:p.Phe4927=
XM_011518466.1:c.14772C=	XP_011516768.1:p.Phe4924=
XM_011518467.1:c.14727C=	XP_011516769.1:p.Phe4909=
NM_001291815.2:c.14904C= MANE Select	NP_001278744.1:p.Phe4968=
XM_011518465.2:c.14781C=	XP_011516767.1:p.Phe4927=
XM_011518466.2:c.14772C=	XP_011516768.1:p.Phe4924=
XM_011518467.2:c.14727C=	XP_011516769.1:p.Phe4909=
XM_017014585.1:c.11685C=	XP_016870074.1:p.Phe3895=
XM_017014586.1:c.7482C=	XP_016870075.1:p.Phe2494=
XR_001746957.1:n.92+264G=
XR_001746958.1:n.92+264G=