Canonical Allele Identifier: CA1881266368

Gene: HMCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433452T= , CM000671.2:g.130433452T=	GRCh38
NC_000009.11:g.133308839T= , CM000671.1:g.133308839T=	GRCh37
NC_000009.10:g.132298660T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14942T=	ENSP00000485357.2:p.Val4981=
ENST00000683500.2:c.14999T= MANE Select	ENSP00000508292.2:p.Val5000=
ENST00000623487.1:n.3345T=
ENST00000624552.3:c.14939T=	ENSP00000485357.1:p.Val4980=
NM_001291815.1:c.14999T=	NP_001278744.1:p.Val5000=
XM_011518465.1:c.14876T=	XP_011516767.1:p.Val4959=
XM_011518466.1:c.14867T=	XP_011516768.1:p.Val4956=
XM_011518467.1:c.14822T=	XP_011516769.1:p.Val4941=
NM_001291815.2:c.14999T= MANE Select	NP_001278744.1:p.Val5000=
XM_011518465.2:c.14876T=	XP_011516767.1:p.Val4959=
XM_011518466.2:c.14867T=	XP_011516768.1:p.Val4956=
XM_011518467.2:c.14822T=	XP_011516769.1:p.Val4941=
XM_017014585.1:c.11780T=	XP_016870074.1:p.Val3927=
XM_017014586.1:c.7577T=	XP_016870075.1:p.Val2526=
XR_001746957.1:n.92+169A=
XR_001746958.1:n.92+169A=