Canonical Allele Identifier: CA805666140

Gene: GPX3

Linked Data

• dbSNP Id: rs1187556261
• gnomAD v4: 5-151028301-G-A
• MyVariant Identifiers: chr5:g.150407862G>A (hg19) ; chr5:g.151028301G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151028301G>A , CM000667.2:g.151028301G>A	GRCh38
NC_000005.9:g.150407862G>A , CM000667.1:g.150407862G>A	GRCh37
NC_000005.8:g.150388055G>A	NCBI36
NG_030590.1:g.64360C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000388825.9:c.*171G>A MANE Select	ENSP00000373477.4:n.*171G>A
ENST00000388825.8:c.*171G>A	ENSP00000373477.4:n.*171G>A
ENST00000521632.1:c.661G>A
ENST00000614343.4:c.*633G>A	ENSP00000483660.1:n.*633G>A
ENST00000622181.4:c.*171G>A	ENSP00000484258.1:n.*171G>A
NM_002084.3:c.*171G>A	NP_002075.2:n.*171G>A
NM_001329790.1:c.*171G>A	NP_001316719.1:n.*171G>A
NM_002084.4:c.*171G>A	NP_002075.2:n.*171G>A
NM_002084.5:c.*171G>A MANE Select	NP_002075.2:n.*171G>A
NM_001329790.2:c.*171G>A	NP_001316719.1:n.*171G>A