Canonical Allele Identifier: CA1881265877

Gene: HMCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433141C= , CM000671.2:g.130433141C=	GRCh38
NC_000009.11:g.133308528C= , CM000671.1:g.133308528C=	GRCh37
NC_000009.10:g.132298349C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14838-207C=	ENSP00000485357.2:n.14838-207C=
ENST00000683500.2:c.14895-207C= MANE Select	ENSP00000508292.2:n.14895-207C=
ENST00000623487.1:n.3034C=
ENST00000624552.3:c.14835-207C=	ENSP00000485357.1:n.14835-207C=
NM_001291815.1:c.14895-207C=	NP_001278744.1:n.14895-207C=
XM_011518465.1:c.14772-207C=	XP_011516767.1:n.14772-207C=
XM_011518466.1:c.14763-207C=	XP_011516768.1:n.14763-207C=
XM_011518467.1:c.14718-207C=	XP_011516769.1:n.14718-207C=
NM_001291815.2:c.14895-207C= MANE Select	NP_001278744.1:n.14895-207C=
XM_011518465.2:c.14772-207C=	XP_011516767.1:n.14772-207C=
XM_011518466.2:c.14763-207C=	XP_011516768.1:n.14763-207C=
XM_011518467.2:c.14718-207C=	XP_011516769.1:n.14718-207C=
XM_017014585.1:c.11676-207C=	XP_016870074.1:n.11676-207C=
XM_017014586.1:c.7473-207C=	XP_016870075.1:n.7473-207C=
XR_001746957.1:n.92+480G=
XR_001746958.1:n.92+480G=