Canonical Allele Identifier: CA375219548

Gene: HMCN2

Linked Data

• gnomAD v4: 9-130433451-G-A
• MyVariant Identifiers: chr9:g.133308838G>A (hg19) ; chr9:g.130433451G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433451G>A , CM000671.2:g.130433451G>A	GRCh38
NC_000009.11:g.133308838G>A , CM000671.1:g.133308838G>A	GRCh37
NC_000009.10:g.132298659G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14941G>A	ENSP00000485357.2:p.Val4981Met
ENST00000683500.2:c.14998G>A MANE Select	ENSP00000508292.2:p.Val5000Met
ENST00000623487.1:n.3344G>A
ENST00000624552.3:c.14938G>A	ENSP00000485357.1:p.Val4980Met
NM_001291815.1:c.14998G>A	NP_001278744.1:p.Val5000Met
XM_011518465.1:c.14875G>A	XP_011516767.1:p.Val4959Met
XM_011518466.1:c.14866G>A	XP_011516768.1:p.Val4956Met
XM_011518467.1:c.14821G>A	XP_011516769.1:p.Val4941Met
NM_001291815.2:c.14998G>A MANE Select	NP_001278744.1:p.Val5000Met
XM_011518465.2:c.14875G>A	XP_011516767.1:p.Val4959Met
XM_011518466.2:c.14866G>A	XP_011516768.1:p.Val4956Met
XM_011518467.2:c.14821G>A	XP_011516769.1:p.Val4941Met
XM_017014585.1:c.11779G>A	XP_016870074.1:p.Val3927Met
XM_017014586.1:c.7576G>A	XP_016870075.1:p.Val2526Met
XR_001746957.1:n.92+170C>T
XR_001746958.1:n.92+170C>T