Canonical Allele Identifier: CA2614646745
Gene: GSTP1 HGNC NCBI

Linked Data

gnomAD v4: 11-67585991-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585991T>C , CM000673.2:g.67585991T>C GRCh38
NC_000011.9:g.67353462T>C , CM000673.1:g.67353462T>C GRCh37
NC_000011.8:g.67110038T>C NCBI36
NG_012075.1:g.7397T>C , LRG_723:g.7397T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000398603.6:c.337-398T>C ENSP00000381604.1:n.337-398T>C
ENST00000398606.10:c.337-113T>C MANE Select ENSP00000381607.3:n.337-113T>C
ENST00000646888.1:c.*53-113T>C ENSP00000494477.1:n.*53-113T>C
ENST00000398603.5:c.337-398T>C ENSP00000381604.1:n.337-398T>C
ENST00000398606.7:c.337-113T>C ENSP00000381607.3:n.337-113T>C
ENST00000467591.1:n.448-113T>C
ENST00000494593.1:n.1132-113T>C
ENST00000498765.5:c.400-113T>C
NM_000852.3:c.337-113T>C , LRG_723t1:c.337-113T>C NP_000843.1:n.337-113T>C
NM_000852.4:c.337-113T>C MANE Select NP_000843.1:n.337-113T>C
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