Canonical Allele Identifier: CA2614645051

Gene: GSTP1

Linked Data

• gnomAD v4: 11-67584811-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67584811_67584812insG , CM000673.2:g.67584811_67584812insG	GRCh38
NC_000011.9:g.67352282_67352283insG , CM000673.1:g.67352282_67352283insG	GRCh37
NC_000011.8:g.67108858_67108859insG	NCBI36
NG_012075.1:g.6217_6218insG , LRG_723:g.6217_6218insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.232+39_232+40insG	ENSP00000381604.1:n.232+39_232+40insG
ENST00000398606.10:c.232+39_232+40insG MANE Select	ENSP00000381607.3:n.232+39_232+40insG
ENST00000646888.1:c.125+39_125+40insG	ENSP00000494477.1:n.125+39_125+40insG
ENST00000398603.5:c.232+39_232+40insG	ENSP00000381604.1:n.232+39_232+40insG
ENST00000398606.7:c.232+39_232+40insG	ENSP00000381607.3:n.232+39_232+40insG
ENST00000467591.1:n.17_18insG
ENST00000489040.1:n.270_271insG
ENST00000494593.1:n.701_702insG
ENST00000498765.5:c.195+39_195+40insG
NM_000852.3:c.232+39_232+40insG , LRG_723t1:c.232+39_232+40insG	NP_000843.1:n.232+39_232+40insG
NM_000852.4:c.232+39_232+40insG MANE Select	NP_000843.1:n.232+39_232+40insG