Canonical Allele Identifier: CA1881266291

Gene: HMCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433417G= , CM000671.2:g.130433417G=	GRCh38
NC_000009.11:g.133308804G= , CM000671.1:g.133308804G=	GRCh37
NC_000009.10:g.132298625G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14907G=	ENSP00000485357.2:p.Leu4969=
ENST00000683500.2:c.14964G= MANE Select	ENSP00000508292.2:p.Leu4988=
ENST00000623487.1:n.3310G=
ENST00000624552.3:c.14904G=	ENSP00000485357.1:p.Leu4968=
NM_001291815.1:c.14964G=	NP_001278744.1:p.Leu4988=
XM_011518465.1:c.14841G=	XP_011516767.1:p.Leu4947=
XM_011518466.1:c.14832G=	XP_011516768.1:p.Leu4944=
XM_011518467.1:c.14787G=	XP_011516769.1:p.Leu4929=
NM_001291815.2:c.14964G= MANE Select	NP_001278744.1:p.Leu4988=
XM_011518465.2:c.14841G=	XP_011516767.1:p.Leu4947=
XM_011518466.2:c.14832G=	XP_011516768.1:p.Leu4944=
XM_011518467.2:c.14787G=	XP_011516769.1:p.Leu4929=
XM_017014585.1:c.11745G=	XP_016870074.1:p.Leu3915=
XM_017014586.1:c.7542G=	XP_016870075.1:p.Leu2514=
XR_001746957.1:n.92+204C=
XR_001746958.1:n.92+204C=