Canonical Allele Identifier: CA600237032
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs1188889088
gnomAD v2: 11-67353352-TA-T
gnomAD v3: 11-67585881-TA-T
gnomAD v4: 11-67585881-TA-T
MyVariant Identifiers: chr11:g.67353353del (hg19) chr11:g.67585882del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585884del , CM000673.2:g.67585884del GRCh38
NC_000011.9:g.67353355del , CM000673.1:g.67353355del GRCh37
NC_000011.8:g.67109931del NCBI36
NG_012075.1:g.7290del , LRG_723:g.7290del

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-505del ENSP00000381604.1:n.337-505del
ENST00000398606.10:c.337-220del MANE Select ENSP00000381607.3:n.337-220del
ENST00000646888.1:c.*53-220del ENSP00000494477.1:n.*53-220del
ENST00000398603.5:c.337-505del ENSP00000381604.1:n.337-505del
ENST00000398606.7:c.337-220del ENSP00000381607.3:n.337-220del
ENST00000467591.1:n.448-220del
ENST00000494593.1:n.1132-220del
ENST00000498765.5:c.400-220del
NM_000852.3:c.337-220del , LRG_723t1:c.337-220del NP_000843.1:n.337-220del
NM_000852.4:c.337-220del MANE Select NP_000843.1:n.337-220del
Search 100 bp 5'
Search 100 bp 3'