Canonical Allele Identifier: CA1591210064
Gene: GPX3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151028377_151028379delinsACG , CM000667.2:g.151028377_151028379delinsACG GRCh38
NC_000005.9:g.150407938_150407940delinsACG , CM000667.1:g.150407938_150407940delinsACG GRCh37
NC_000005.8:g.150388131_150388133delinsACG NCBI36
NG_030590.1:g.64282_64284delinsCGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000388825.9:c.*247_*249delinsACG MANE Select ENSP00000373477.4:n.*247_*249delinsACG
ENST00000388825.8:c.*247_*249delinsACG ENSP00000373477.4:n.*247_*249delinsACG
ENST00000521632.1:c.737_739delinsACG
ENST00000614343.4:c.*709_*711delinsACG ENSP00000483660.1:n.*709_*711delinsACG
ENST00000622181.4:c.*247_*249delinsACG ENSP00000484258.1:n.*247_*249delinsACG
NM_002084.3:c.*247_*249delinsACG NP_002075.2:n.*247_*249delinsACG
NM_001329790.1:c.*247_*249delinsACG NP_001316719.1:n.*247_*249delinsACG
NM_002084.4:c.*247_*249delinsACG NP_002075.2:n.*247_*249delinsACG
NM_002084.5:c.*247_*249delinsACG MANE Select NP_002075.2:n.*247_*249delinsACG
NM_001329790.2:c.*247_*249delinsACG NP_001316719.1:n.*247_*249delinsACG
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