Canonical Allele Identifier: CA12012925
Gene: GPX3 HGNC NCBI

Linked Data

dbSNP Id: rs8177441
gnomAD v2: 5-150405994-G-C
gnomAD v3: 5-151026433-G-C
gnomAD v4: 5-151026433-G-C
MyVariant Identifiers: chr5:g.150405994G>C (hg19) chr5:g.151026433G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151026433G>C , CM000667.2:g.151026433G>C GRCh38
NC_000005.9:g.150405994G>C , CM000667.1:g.150405994G>C GRCh37
NC_000005.8:g.150386187G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000388825.9:c.242-467G>C MANE Select ENSP00000373477.4:n.242-467G>C
ENST00000388825.8:c.242-467G>C ENSP00000373477.4:n.242-467G>C
ENST00000517973.1:c.88-467G>C ENSP00000429709.1:n.88-467G>C
ENST00000519214.5:c.*476-467G>C ENSP00000430508.1:n.*476-467G>C
ENST00000521632.1:c.151-467G>C
ENST00000521650.5:c.269-467G>C ENSP00000427873.1:n.269-467G>C
ENST00000521722.5:n.305-278G>C
ENST00000614343.4:c.*23-467G>C ENSP00000483660.1:n.*23-467G>C
ENST00000622181.4:c.239-467G>C ENSP00000484258.1:n.239-467G>C
NM_002084.3:c.242-467G>C NP_002075.2:n.242-467G>C
NM_001329790.1:c.269-467G>C NP_001316719.1:n.269-467G>C
NM_002084.4:c.242-467G>C NP_002075.2:n.242-467G>C
NM_002084.5:c.242-467G>C MANE Select NP_002075.2:n.242-467G>C
NM_001329790.2:c.269-467G>C NP_001316719.1:n.269-467G>C
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