Canonical Allele Identifier: CA6142718

Gene: GSTP1

Linked Data

• dbSNP Id: rs772969255
• ExAC: 11:67352065 G / GGGAGGGGGT
• gnomAD v2: 11-67352065-G-GGGAGGGGGT
• gnomAD v4: 11-67584594-G-GGGAGGGGGT
• MyVariant Identifiers: chr11:g.67352065_67352066insGGAGGGGGT (hg19) ; chr11:g.67584594_67584595insGGAGGGGGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67584596_67584604dup , CM000673.2:g.67584596_67584604dup	GRCh38
NC_000011.9:g.67352067_67352075dup , CM000673.1:g.67352067_67352075dup	GRCh37
NC_000011.8:g.67108643_67108651dup	NCBI36
NG_012075.1:g.6002_6010dup , LRG_723:g.6002_6010dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.144+26_144+34dup	ENSP00000381604.1:n.144+26_144+34dup
ENST00000398606.10:c.144+26_144+34dup MANE Select	ENSP00000381607.3:n.144+26_144+34dup
ENST00000646888.1:c.38-89_38-81dup	ENSP00000494477.1:n.38-89_38-81dup
ENST00000398603.5:c.144+26_144+34dup	ENSP00000381604.1:n.144+26_144+34dup
ENST00000398606.7:c.144+26_144+34dup	ENSP00000381607.3:n.144+26_144+34dup
ENST00000489040.1:n.143+26_143+34dup
ENST00000494593.1:n.486_494dup
ENST00000498765.5:c.107+26_107+34dup
NM_000852.3:c.144+26_144+34dup , LRG_723t1:c.144+26_144+34dup	NP_000843.1:n.144+26_144+34dup
NM_000852.4:c.144+26_144+34dup MANE Select	NP_000843.1:n.144+26_144+34dup