Canonical Allele Identifier: CA381516086
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67352212T>A (hg19) chr11:g.67584741T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67584741T>A , CM000673.2:g.67584741T>A GRCh38
NC_000011.9:g.67352212T>A , CM000673.1:g.67352212T>A GRCh37
NC_000011.8:g.67108788T>A NCBI36
NG_012075.1:g.6147T>A , LRG_723:g.6147T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.201T>A ENSP00000381604.1:p.Asn67Lys
ENST00000398606.10:c.201T>A MANE Select ENSP00000381607.3:p.Asn67Lys
ENST00000646888.1:c.94T>A ENSP00000494477.1:p.Tyr32Asn
ENST00000398603.5:c.201T>A ENSP00000381604.1:p.Asn67Lys
ENST00000398606.7:c.201T>A ENSP00000381607.3:p.Asn67Lys
ENST00000489040.1:n.200T>A
ENST00000494593.1:n.631T>A
ENST00000498765.5:c.164T>A
NM_000852.3:c.201T>A , LRG_723t1:c.201T>A NP_000843.1:p.Asn67Lys
NM_000852.4:c.201T>A MANE Select NP_000843.1:p.Asn67Lys
Search 100 bp 5'
Search 100 bp 3'