Canonical Allele Identifier: CA129883299
Gene: GPX3 HGNC NCBI

Linked Data

dbSNP Id: rs7722386
MyVariant Identifiers: chr5:g.150407852A>G (hg19) chr5:g.151028291A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151028291A>G , CM000667.2:g.151028291A>G GRCh38
NC_000005.9:g.150407852A>G , CM000667.1:g.150407852A>G GRCh37
NC_000005.8:g.150388045A>G NCBI36
NG_030590.1:g.64370T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000388825.9:c.*161A>G MANE Select ENSP00000373477.4:n.*161A>G
ENST00000388825.8:c.*161A>G ENSP00000373477.4:n.*161A>G
ENST00000521632.1:c.651A>G
ENST00000614343.4:c.*623A>G ENSP00000483660.1:n.*623A>G
ENST00000622181.4:c.*161A>G ENSP00000484258.1:n.*161A>G
NM_002084.3:c.*161A>G NP_002075.2:n.*161A>G
NM_001329790.1:c.*161A>G NP_001316719.1:n.*161A>G
NM_002084.4:c.*161A>G NP_002075.2:n.*161A>G
NM_002084.5:c.*161A>G MANE Select NP_002075.2:n.*161A>G
NM_001329790.2:c.*161A>G NP_001316719.1:n.*161A>G
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