Canonical Allele Identifier: CA375219462

Gene: HMCN2

Linked Data

• gnomAD v4: 9-130433433-G-A
• MyVariant Identifiers: chr9:g.133308820G>A (hg19) ; chr9:g.130433433G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433433G>A , CM000671.2:g.130433433G>A	GRCh38
NC_000009.11:g.133308820G>A , CM000671.1:g.133308820G>A	GRCh37
NC_000009.10:g.132298641G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14923G>A	ENSP00000485357.2:p.Val4975Met
ENST00000683500.2:c.14980G>A MANE Select	ENSP00000508292.2:p.Val4994Met
ENST00000623487.1:n.3326G>A
ENST00000624552.3:c.14920G>A	ENSP00000485357.1:p.Val4974Met
NM_001291815.1:c.14980G>A	NP_001278744.1:p.Val4994Met
XM_011518465.1:c.14857G>A	XP_011516767.1:p.Val4953Met
XM_011518466.1:c.14848G>A	XP_011516768.1:p.Val4950Met
XM_011518467.1:c.14803G>A	XP_011516769.1:p.Val4935Met
NM_001291815.2:c.14980G>A MANE Select	NP_001278744.1:p.Val4994Met
XM_011518465.2:c.14857G>A	XP_011516767.1:p.Val4953Met
XM_011518466.2:c.14848G>A	XP_011516768.1:p.Val4950Met
XM_011518467.2:c.14803G>A	XP_011516769.1:p.Val4935Met
XM_017014585.1:c.11761G>A	XP_016870074.1:p.Val3921Met
XM_017014586.1:c.7558G>A	XP_016870075.1:p.Val2520Met
XR_001746957.1:n.92+188C>T
XR_001746958.1:n.92+188C>T