Canonical Allele Identifier: CA1881266177

Gene: HMCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433368C= , CM000671.2:g.130433368C=	GRCh38
NC_000009.11:g.133308755C= , CM000671.1:g.133308755C=	GRCh37
NC_000009.10:g.132298576C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14858C=	ENSP00000485357.2:p.Ser4953=
ENST00000683500.2:c.14915C= MANE Select	ENSP00000508292.2:p.Ser4972=
ENST00000623487.1:n.3261C=
ENST00000624552.3:c.14855C=	ENSP00000485357.1:p.Ser4952=
NM_001291815.1:c.14915C=	NP_001278744.1:p.Ser4972=
XM_011518465.1:c.14792C=	XP_011516767.1:p.Ser4931=
XM_011518466.1:c.14783C=	XP_011516768.1:p.Ser4928=
XM_011518467.1:c.14738C=	XP_011516769.1:p.Ser4913=
NM_001291815.2:c.14915C= MANE Select	NP_001278744.1:p.Ser4972=
XM_011518465.2:c.14792C=	XP_011516767.1:p.Ser4931=
XM_011518466.2:c.14783C=	XP_011516768.1:p.Ser4928=
XM_011518467.2:c.14738C=	XP_011516769.1:p.Ser4913=
XM_017014585.1:c.11696C=	XP_016870074.1:p.Ser3899=
XM_017014586.1:c.7493C=	XP_016870075.1:p.Ser2498=
XR_001746957.1:n.92+253G=
XR_001746958.1:n.92+253G=