Canonical Allele Identifier: CA2676036194
Gene: GPX3 HGNC NCBI

Linked Data

gnomAD v4: 5-151028382-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151028382T>C , CM000667.2:g.151028382T>C GRCh38
NC_000005.9:g.150407943T>C , CM000667.1:g.150407943T>C GRCh37
NC_000005.8:g.150388136T>C NCBI36
NG_030590.1:g.64279A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000388825.9:c.*252T>C MANE Select ENSP00000373477.4:n.*252T>C
ENST00000388825.8:c.*252T>C ENSP00000373477.4:n.*252T>C
ENST00000521632.1:c.742T>C
ENST00000614343.4:c.*714T>C ENSP00000483660.1:n.*714T>C
ENST00000622181.4:c.*252T>C ENSP00000484258.1:n.*252T>C
NM_002084.3:c.*252T>C NP_002075.2:n.*252T>C
NM_001329790.1:c.*252T>C NP_001316719.1:n.*252T>C
NM_002084.4:c.*252T>C NP_002075.2:n.*252T>C
NM_002084.5:c.*252T>C MANE Select NP_002075.2:n.*252T>C
NM_001329790.2:c.*252T>C NP_001316719.1:n.*252T>C
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