Canonical Allele Identifier: CA1980213825

Gene: GSTP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67584656_67584671delinsCCCTCCCTGAGCCATG , CM000673.2:g.67584656_67584671delinsCCCTCCCTGAGCCATG	GRCh38
NC_000011.9:g.67352127_67352142delinsCCCTCCCTGAGCCATG , CM000673.1:g.67352127_67352142delinsCCCTCCCTGAGCCATG	GRCh37
NC_000011.8:g.67108703_67108718delinsCCCTCCCTGAGCCATG	NCBI36
NG_012075.1:g.6062_6077delinsCCCTCCCTGAGCCATG , LRG_723:g.6062_6077delinsCCCTCCCTGAGCCATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.145-29_145-14delinsCCCTCCCTGAGCCATG	ENSP00000381604.1:n.145-29_145-14delinsCCCTCCCTGAGCCATG
ENST00000398606.10:c.145-29_145-14delinsCCCTCCCTGAGCCATG MANE Select	ENSP00000381607.3:n.145-29_145-14delinsCCCTCCCTGAGCCATG
ENST00000646888.1:c.38-29_38-14delinsCCCTCCCTGAGCCATG	ENSP00000494477.1:n.38-29_38-14delinsCCCTCCCTGAGCCATG
ENST00000398603.5:c.145-29_145-14delinsCCCTCCCTGAGCCATG	ENSP00000381604.1:n.145-29_145-14delinsCCCTCCCTGAGCCATG
ENST00000398606.7:c.145-29_145-14delinsCCCTCCCTGAGCCATG	ENSP00000381607.3:n.145-29_145-14delinsCCCTCCCTGAGCCATG
ENST00000489040.1:n.144-29_144-14delinsCCCTCCCTGAGCCATG
ENST00000494593.1:n.546_561delinsCCCTCCCTGAGCCATG
ENST00000498765.5:c.108-29_108-14delinsCCCTCCCTGAGCCATG
NM_000852.3:c.145-29_145-14delinsCCCTCCCTGAGCCATG , LRG_723t1:c.145-29_145-14delinsCCCTCCCTGAGCCATG	NP_000843.1:n.145-29_145-14delinsCCCTCCCTGAGCCATG
NM_000852.4:c.145-29_145-14delinsCCCTCCCTGAGCCATG MANE Select	NP_000843.1:n.145-29_145-14delinsCCCTCCCTGAGCCATG