Canonical Allele Identifier: CA2614641999
Gene: GSTP1 HGNC NCBI

Linked Data

gnomAD v4: 11-67583829-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67583829G>C , CM000673.2:g.67583829G>C GRCh38
NC_000011.9:g.67351300G>C , CM000673.1:g.67351300G>C GRCh37
NC_000011.8:g.67107876G>C NCBI36
NG_012075.1:g.5235G>C , LRG_723:g.5235G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000398603.6:c.-15G>C ENSP00000381604.1:n.-15G>C
ENST00000398606.10:c.-15G>C MANE Select ENSP00000381607.3:n.-15G>C
ENST00000646888.1:c.-15G>C ENSP00000494477.1:n.-15G>C
ENST00000398603.5:c.-15G>C ENSP00000381604.1:n.-15G>C
ENST00000398606.7:c.-15G>C ENSP00000381607.3:n.-15G>C
ENST00000494593.1:n.8G>C
NM_000852.3:c.-15G>C , LRG_723t1:c.-15G>C NP_000843.1:n.-15G>C
NM_000852.4:c.-15G>C MANE Select NP_000843.1:n.-15G>C
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