Canonical Allele Identifier: CA600237068

Gene: GSTP1

Linked Data

• dbSNP Id: rs1314194754
• gnomAD v2: 11-67353595-TGTGAAG-T
• gnomAD v4: 11-67586124-TGTGAAG-T
• MyVariant Identifiers: chr11:g.67353596_67353601del (hg19) ; chr11:g.67586125_67586130del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586126_67586131del , CM000673.2:g.67586126_67586131del	GRCh38
NC_000011.9:g.67353597_67353602del , CM000673.1:g.67353597_67353602del	GRCh37
NC_000011.8:g.67110173_67110178del	NCBI36
NG_012075.1:g.7532_7537del , LRG_723:g.7532_7537del

Transcript Alleles

HGVS	Amino-acid change
ENST00000398603.6:c.337-263_337-258del	ENSP00000381604.1:n.337-263_337-258del
ENST00000398606.10:c.359_364del MANE Select	ENSP00000381607.3:p.Val120_Lys121del
ENST00000646888.1:c.*75_*80del	ENSP00000494477.1:n.*75_*80del
ENST00000398603.5:c.337-263_337-258del	ENSP00000381604.1:n.337-263_337-258del
ENST00000398606.7:c.359_364del	ENSP00000381607.3:p.Val120_Lys121del
ENST00000467591.1:n.470_475del
ENST00000494593.1:n.1154_1159del
ENST00000495996.1:c.23_28del	ENSP00000484686.1:p.Val8_Lys9del
ENST00000498765.5:c.422_427del
NM_000852.3:c.359_364del , LRG_723t1:c.359_364del	NP_000843.1:p.Val120_Lys121del
NM_000852.4:c.359_364del MANE Select	NP_000843.1:p.Val120_Lys121del