Canonical Allele Identifier: CA1980215914
Gene: GSTP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586123_67586125delinsATG , CM000673.2:g.67586123_67586125delinsATG GRCh38
NC_000011.9:g.67353594_67353596delinsATG , CM000673.1:g.67353594_67353596delinsATG GRCh37
NC_000011.8:g.67110170_67110172delinsATG NCBI36
NG_012075.1:g.7529_7531delinsATG , LRG_723:g.7529_7531delinsATG

Transcript Alleles

HGVS Amino-acid change
ENST00000398603.6:c.337-266_337-264delinsATG ENSP00000381604.1:n.337-266_337-264delins...
ENST00000398606.10:c.356_358delinsATG MANE Select ENSP00000381607.3:p.Tyr119=
ENST00000646888.1:c.*72_*74delinsATG ENSP00000494477.1:n.*72_*74delinsATG
ENST00000398603.5:c.337-266_337-264delinsATG ENSP00000381604.1:n.337-266_337-264delins...
ENST00000398606.7:c.356_358delinsATG ENSP00000381607.3:p.Tyr119=
ENST00000467591.1:n.467_469delinsATG
ENST00000494593.1:n.1151_1153delinsATG
ENST00000495996.1:c.20_22delinsATG ENSP00000484686.1:p.Tyr7=
ENST00000498765.5:c.419_421delinsATG
NM_000852.3:c.356_358delinsATG , LRG_723t1:c.356_358delinsATG NP_000843.1:p.Tyr119=
NM_000852.4:c.356_358delinsATG MANE Select NP_000843.1:p.Tyr119=