Canonical Allele Identifier: CA6142731

Gene: GSTP1

Linked Data

• dbSNP Id: rs760238027
• ExAC: 11:67352127 CCCTCCCTGAGCCATG / C
• gnomAD v2: 11-67352127-CCCTCCCTGAGCCATG-C
• gnomAD v4: 11-67584656-CCCTCCCTGAGCCATG-C
• MyVariant Identifiers: chr11:g.67352128_67352142del (hg19) ; chr11:g.67584657_67584671del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67584663_67584677del , CM000673.2:g.67584663_67584677del	GRCh38
NC_000011.9:g.67352134_67352148del , CM000673.1:g.67352134_67352148del	GRCh37
NC_000011.8:g.67108710_67108724del	NCBI36
NG_012075.1:g.6069_6083del , LRG_723:g.6069_6083del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.145-22_145-8del	ENSP00000381604.1:n.145-22_145-8del
ENST00000398606.10:c.145-22_145-8del MANE Select	ENSP00000381607.3:n.145-22_145-8del
ENST00000646888.1:c.38-22_38-8del	ENSP00000494477.1:n.38-22_38-8del
ENST00000398603.5:c.145-22_145-8del	ENSP00000381604.1:n.145-22_145-8del
ENST00000398606.7:c.145-22_145-8del	ENSP00000381607.3:n.145-22_145-8del
ENST00000489040.1:n.144-22_144-8del
ENST00000494593.1:n.553_567del
ENST00000498765.5:c.108-22_108-8del
NM_000852.3:c.145-22_145-8del , LRG_723t1:c.145-22_145-8del	NP_000843.1:n.145-22_145-8del
NM_000852.4:c.145-22_145-8del MANE Select	NP_000843.1:n.145-22_145-8del