Canonical Allele Identifier: CA375219412

Gene: HMCN2

Linked Data

• gnomAD v4: 9-130433419-C-A
• COSMIC: COSM6389527
• MyVariant Identifiers: chr9:g.133308806C>A (hg19) ; chr9:g.130433419C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433419C>A , CM000671.2:g.130433419C>A	GRCh38
NC_000009.11:g.133308806C>A , CM000671.1:g.133308806C>A	GRCh37
NC_000009.10:g.132298627C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14909C>A	ENSP00000485357.2:p.Pro4970Gln
ENST00000683500.2:c.14966C>A MANE Select	ENSP00000508292.2:p.Pro4989Gln
ENST00000623487.1:n.3312C>A
ENST00000624552.3:c.14906C>A	ENSP00000485357.1:p.Pro4969Gln
NM_001291815.1:c.14966C>A	NP_001278744.1:p.Pro4989Gln
XM_011518465.1:c.14843C>A	XP_011516767.1:p.Pro4948Gln
XM_011518466.1:c.14834C>A	XP_011516768.1:p.Pro4945Gln
XM_011518467.1:c.14789C>A	XP_011516769.1:p.Pro4930Gln
NM_001291815.2:c.14966C>A MANE Select	NP_001278744.1:p.Pro4989Gln
XM_011518465.2:c.14843C>A	XP_011516767.1:p.Pro4948Gln
XM_011518466.2:c.14834C>A	XP_011516768.1:p.Pro4945Gln
XM_011518467.2:c.14789C>A	XP_011516769.1:p.Pro4930Gln
XM_017014585.1:c.11747C>A	XP_016870074.1:p.Pro3916Gln
XM_017014586.1:c.7544C>A	XP_016870075.1:p.Pro2515Gln
XR_001746957.1:n.92+202G>T
XR_001746958.1:n.92+202G>T