Canonical Allele Identifier: CA375219229

Gene: HMCN2

Linked Data

• MyVariant Identifiers: chr9:g.133308761A>T (hg19) ; chr9:g.130433374A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433374A>T , CM000671.2:g.130433374A>T	GRCh38
NC_000009.11:g.133308761A>T , CM000671.1:g.133308761A>T	GRCh37
NC_000009.10:g.132298582A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14864A>T	ENSP00000485357.2:p.Asp4955Val
ENST00000683500.2:c.14921A>T MANE Select	ENSP00000508292.2:p.Asp4974Val
ENST00000623487.1:n.3267A>T
ENST00000624552.3:c.14861A>T	ENSP00000485357.1:p.Asp4954Val
NM_001291815.1:c.14921A>T	NP_001278744.1:p.Asp4974Val
XM_011518465.1:c.14798A>T	XP_011516767.1:p.Asp4933Val
XM_011518466.1:c.14789A>T	XP_011516768.1:p.Asp4930Val
XM_011518467.1:c.14744A>T	XP_011516769.1:p.Asp4915Val
NM_001291815.2:c.14921A>T MANE Select	NP_001278744.1:p.Asp4974Val
XM_011518465.2:c.14798A>T	XP_011516767.1:p.Asp4933Val
XM_011518466.2:c.14789A>T	XP_011516768.1:p.Asp4930Val
XM_011518467.2:c.14744A>T	XP_011516769.1:p.Asp4915Val
XM_017014585.1:c.11702A>T	XP_016870074.1:p.Asp3901Val
XM_017014586.1:c.7499A>T	XP_016870075.1:p.Asp2500Val
XR_001746957.1:n.92+247T>A
XR_001746958.1:n.92+247T>A