Canonical Allele Identifier: CA15381790
Gene: GPX3 HGNC NCBI

Linked Data

dbSNP Id: rs3805435

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151021735T>C , CM000667.2:g.151021735T>C GRCh38
NC_000005.9:g.150401296T>C , CM000667.1:g.150401296T>C GRCh37
NC_000005.8:g.150381489T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000388825.9:c.87+994T>C MANE Select ENSP00000373477.4:n.87+994T>C
ENST00000388825.8:c.87+994T>C ENSP00000373477.4:n.87+994T>C
ENST00000517973.1:c.87+994T>C ENSP00000429709.1:n.87+994T>C
ENST00000519214.5:c.*321+482T>C ENSP00000430508.1:n.*321+482T>C
ENST00000521650.5:c.114+881T>C ENSP00000427873.1:n.114+881T>C
ENST00000521722.5:n.150+994T>C
ENST00000614343.4:c.87+994T>C ENSP00000483660.1:n.87+994T>C
ENST00000622181.4:c.87+994T>C ENSP00000484258.1:n.87+994T>C
ENST00000625178.1:n.299T>C
NM_002084.3:c.87+994T>C NP_002075.2:n.87+994T>C
NM_001329790.1:c.114+881T>C NP_001316719.1:n.114+881T>C
NM_002084.4:c.87+994T>C NP_002075.2:n.87+994T>C
NM_002084.5:c.87+994T>C MANE Select NP_002075.2:n.87+994T>C
NM_001329790.2:c.114+881T>C NP_001316719.1:n.114+881T>C