Canonical Allele Identifier: CA1881266423

Gene: HMCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433474C= , CM000671.2:g.130433474C=	GRCh38
NC_000009.11:g.133308861C= , CM000671.1:g.133308861C=	GRCh37
NC_000009.10:g.132298682C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14964C=	ENSP00000485357.2:p.Ser4988=
ENST00000683500.2:c.15021C= MANE Select	ENSP00000508292.2:p.Ser5007=
ENST00000623487.1:n.3367C=
ENST00000624552.3:c.14961C=	ENSP00000485357.1:p.Ser4987=
NM_001291815.1:c.15021C=	NP_001278744.1:p.Ser5007=
XM_011518465.1:c.14898C=	XP_011516767.1:p.Ser4966=
XM_011518466.1:c.14889C=	XP_011516768.1:p.Ser4963=
XM_011518467.1:c.14844C=	XP_011516769.1:p.Ser4948=
NM_001291815.2:c.15021C= MANE Select	NP_001278744.1:p.Ser5007=
XM_011518465.2:c.14898C=	XP_011516767.1:p.Ser4966=
XM_011518466.2:c.14889C=	XP_011516768.1:p.Ser4963=
XM_011518467.2:c.14844C=	XP_011516769.1:p.Ser4948=
XM_017014585.1:c.11802C=	XP_016870074.1:p.Ser3934=
XM_017014586.1:c.7599C=	XP_016870075.1:p.Ser2533=
XR_001746957.1:n.92+147G=
XR_001746958.1:n.92+147G=