Canonical Allele Identifier: CA1591210077
Community Standard Title: NM_002084.5(GPX3):c.*249G>C
Gene: GPX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151028379G>C , CM000667.2:g.151028379G>C GRCh38
NC_000005.9:g.150407940G>C , CM000667.1:g.150407940G>C GRCh37
NC_000005.8:g.150388133G>C NCBI36
NG_030590.1:g.64282C>G

Transcript Alleles

HGVS Amino-acid Change
NM_002084.5:c.*249G>C MANE Select NP_002075.2:n.*249G>C
ENST00000388825.9:c.*249G>C MANE Select ENSP00000373477.4:n.*249G>C
NM_001329790.1:c.*249G>C NP_001316719.1:n.*249G>C
NM_001329790.2:c.*249G>C NP_001316719.1:n.*249G>C
NM_002084.3:c.*249G>C NP_002075.2:n.*249G>C
NM_002084.4:c.*249G>C NP_002075.2:n.*249G>C
ENST00000388825.8:c.*249G>C ENSP00000373477.4:n.*249G>C
ENST00000521632.1:c.739G>C
ENST00000614343.4:c.*711G>C ENSP00000483660.1:n.*711G>C
ENST00000622181.4:c.*249G>C ENSP00000484258.1:n.*249G>C