Canonical Allele Identifier: CA381521621
Gene: GSTP1 HGNC NCBI

Linked Data

gnomAD v4: 11-67586215-A-C
MyVariant Identifiers: chr11:g.67353686A>C (hg19) chr11:g.67586215A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586215A>C , CM000673.2:g.67586215A>C GRCh38
NC_000011.9:g.67353686A>C , CM000673.1:g.67353686A>C GRCh37
NC_000011.8:g.67110262A>C NCBI36
NG_012075.1:g.7621A>C , LRG_723:g.7621A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-174A>C ENSP00000381604.1:n.337-174A>C
ENST00000398606.10:c.444+4A>C MANE Select ENSP00000381607.3:n.444+4A>C
ENST00000646888.1:c.*160+4A>C ENSP00000494477.1:n.*160+4A>C
ENST00000398603.5:c.337-174A>C ENSP00000381604.1:n.337-174A>C
ENST00000398606.7:c.444+4A>C ENSP00000381607.3:n.444+4A>C
ENST00000467591.1:n.555+4A>C
ENST00000494593.1:n.1243A>C
ENST00000495996.1:c.112A>C ENSP00000484686.1:p.Ser38Arg
ENST00000498765.5:c.507+4A>C
NM_000852.3:c.444+4A>C , LRG_723t1:c.444+4A>C NP_000843.1:n.444+4A>C
NM_000852.4:c.444+4A>C MANE Select NP_000843.1:n.444+4A>C
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