Canonical Allele Identifier: CA381522966
Gene: GSTP1 HGNC NCBI

Linked Data

gnomAD v4: 11-67586494-C-A
MyVariant Identifiers: chr11:g.67353965C>A (hg19) chr11:g.67586494C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586494C>A , CM000673.2:g.67586494C>A GRCh38
NC_000011.9:g.67353965C>A , CM000673.1:g.67353965C>A GRCh37
NC_000011.8:g.67110541C>A NCBI36
NG_012075.1:g.7900C>A , LRG_723:g.7900C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.442C>A ENSP00000381604.1:p.Leu148Ile
ENST00000398606.10:c.550C>A MANE Select ENSP00000381607.3:p.Leu184Ile
ENST00000646888.1:c.*266C>A ENSP00000494477.1:n.*266C>A
ENST00000398603.5:c.442C>A ENSP00000381604.1:p.Leu148Ile
ENST00000398606.7:c.550C>A ENSP00000381607.3:p.Leu184Ile
ENST00000467591.1:n.661C>A
ENST00000494593.1:n.1522C>A
ENST00000498765.5:c.613C>A
NM_000852.3:c.550C>A , LRG_723t1:c.550C>A NP_000843.1:p.Leu184Ile
NM_000852.4:c.550C>A MANE Select NP_000843.1:p.Leu184Ile
Search 100 bp 5'
Search 100 bp 3'