Canonical Allele Identifier: CA475396012
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67353607G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586136G>C , CM000673.2:g.67586136G>C GRCh38
NC_000011.9:g.67353607G>C , CM000673.1:g.67353607G>C GRCh37
NC_000011.8:g.67110183G>C NCBI36
NG_012075.1:g.7542G>C , LRG_723:g.7542G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-253G>C ENSP00000381604.1:n.337-253G>C
ENST00000398606.10:c.369G>C MANE Select ENSP00000381607.3:p.Leu123=
ENST00000646888.1:c.*85G>C ENSP00000494477.1:n.*85G>C
ENST00000398603.5:c.337-253G>C ENSP00000381604.1:n.337-253G>C
ENST00000398606.7:c.369G>C ENSP00000381607.3:p.Leu123=
ENST00000467591.1:n.480G>C
ENST00000494593.1:n.1164G>C
ENST00000495996.1:c.33G>C ENSP00000484686.1:p.Leu11=
ENST00000498765.5:c.432G>C
NM_000852.3:c.369G>C , LRG_723t1:c.369G>C NP_000843.1:p.Leu123=
NM_000852.4:c.369G>C MANE Select NP_000843.1:p.Leu123=