Canonical Allele Identifier: CA2676036219

Gene: GPX3

Linked Data

• gnomAD v4: 5-151028392-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151028392T>C , CM000667.2:g.151028392T>C	GRCh38
NC_000005.9:g.150407953T>C , CM000667.1:g.150407953T>C	GRCh37
NC_000005.8:g.150388146T>C	NCBI36
NG_030590.1:g.64269A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388825.9:c.*262T>C MANE Select	ENSP00000373477.4:n.*262T>C
ENST00000388825.8:c.*262T>C	ENSP00000373477.4:n.*262T>C
ENST00000521632.1:c.752T>C
ENST00000614343.4:c.*724T>C	ENSP00000483660.1:n.*724T>C
ENST00000622181.4:c.*262T>C	ENSP00000484258.1:n.*262T>C
NM_002084.3:c.*262T>C	NP_002075.2:n.*262T>C
NM_001329790.1:c.*262T>C	NP_001316719.1:n.*262T>C
NM_002084.4:c.*262T>C	NP_002075.2:n.*262T>C
NM_002084.5:c.*262T>C MANE Select	NP_002075.2:n.*262T>C
NM_001329790.2:c.*262T>C	NP_001316719.1:n.*262T>C