Canonical Allele Identifier: CA2676035961
Gene: GPX3 HGNC NCBI

Linked Data

gnomAD v4: 5-151028294-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151028294C>A , CM000667.2:g.151028294C>A GRCh38
NC_000005.9:g.150407855C>A , CM000667.1:g.150407855C>A GRCh37
NC_000005.8:g.150388048C>A NCBI36
NG_030590.1:g.64367G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000388825.9:c.*164C>A MANE Select ENSP00000373477.4:n.*164C>A
ENST00000388825.8:c.*164C>A ENSP00000373477.4:n.*164C>A
ENST00000521632.1:c.654C>A
ENST00000614343.4:c.*626C>A ENSP00000483660.1:n.*626C>A
ENST00000622181.4:c.*164C>A ENSP00000484258.1:n.*164C>A
NM_002084.3:c.*164C>A NP_002075.2:n.*164C>A
NM_001329790.1:c.*164C>A NP_001316719.1:n.*164C>A
NM_002084.4:c.*164C>A NP_002075.2:n.*164C>A
NM_002084.5:c.*164C>A MANE Select NP_002075.2:n.*164C>A
NM_001329790.2:c.*164C>A NP_001316719.1:n.*164C>A
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