Canonical Allele Identifier: CA381515832
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67352193T>C (hg19) chr11:g.67584722T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584722T>C , CM000673.2:g.67584722T>C GRCh38
NC_000011.9:g.67352193T>C , CM000673.1:g.67352193T>C GRCh37
NC_000011.8:g.67108769T>C NCBI36
NG_012075.1:g.6128T>C , LRG_723:g.6128T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.182T>C ENSP00000381604.1:p.Leu61Pro
ENST00000398606.10:c.182T>C MANE Select ENSP00000381607.3:p.Leu61Pro
ENST00000646888.1:c.75T>C ENSP00000494477.1:p.Pro25=
ENST00000398603.5:c.182T>C ENSP00000381604.1:p.Leu61Pro
ENST00000398606.7:c.182T>C ENSP00000381607.3:p.Leu61Pro
ENST00000489040.1:n.181T>C
ENST00000494593.1:n.612T>C
ENST00000498765.5:c.145T>C
NM_000852.3:c.182T>C , LRG_723t1:c.182T>C NP_000843.1:p.Leu61Pro
NM_000852.4:c.182T>C MANE Select NP_000843.1:p.Leu61Pro
Search 100 bp 5'
Search 100 bp 3'