Canonical Allele Identifier: CA390507673
Gene: GSTZ1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77327535A>T , CM000676.2:g.77327535A>T GRCh38
NC_000014.8:g.77793878A>T , CM000676.1:g.77793878A>T GRCh37
NC_000014.7:g.76863631A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000216465.10:c.199A>T MANE Select ENSP00000216465.5:p.Ile67Phe
ENST00000216465.9:c.199A>T ENSP00000216465.5:p.Ile67Phe
ENST00000349555.7:c.199A>T ENSP00000314404.5:p.Ile67Phe
ENST00000361389.8:c.34A>T ENSP00000354959.4:p.Ile12Phe
ENST00000393734.5:c.34A>T ENSP00000377335.1:p.Ile12Phe
ENST00000553431.5:n.330A>T
ENST00000553586.5:c.202A>T ENSP00000451976.1:p.Ile68Phe
ENST00000553838.5:n.369A>T
ENST00000554279.5:c.174+25A>T ENSP00000452498.1:n.174+25A>T
ENST00000554846.5:c.34A>T ENSP00000452531.1:p.Ile12Phe
ENST00000555093.1:n.4248A>T
ENST00000555583.1:c.34A>T ENSP00000452346.1:p.Ile12Phe
ENST00000556627.5:c.136-377A>T ENSP00000450487.1:n.136-377A>T
ENST00000556914.5:n.279A>T
ENST00000557053.5:c.34A>T ENSP00000451150.1:p.Ile12Phe
ENST00000557639.5:c.34A>T ENSP00000451927.1:p.Ile12Phe
NM_001312660.1:c.34A>T NP_001299589.1:p.Ile12Phe
NM_001513.3:c.34A>T NP_001504.2:p.Ile12Phe
NM_145870.2:c.199A>T NP_665877.1:p.Ile67Phe
NM_145871.2:c.199A>T NP_665878.2:p.Ile67Phe
XM_005267559.2:c.34A>T XP_005267616.1:p.Ile12Phe
XM_011536670.1:c.-278A>T XP_011534972.1:n.-278A>T
XM_011536671.1:c.202A>T XP_011534973.1:p.Ile68Phe
NM_001363703.1:c.202A>T NP_001350632.1:p.Ile68Phe
XM_011536670.2:c.-278A>T XP_011534972.1:n.-278A>T
XM_011536671.2:c.202A>T XP_011534973.1:p.Ile68Phe
XM_024449549.1:c.-278A>T XP_024305317.1:n.-278A>T
XM_024449550.1:c.34A>T XP_024305318.1:p.Ile12Phe
XM_024449551.1:c.34A>T XP_024305319.1:p.Ile12Phe
XM_024449552.1:c.34A>T XP_024305320.1:p.Ile12Phe
NM_145870.3:c.199A>T MANE Select NP_665877.1:p.Ile67Phe
NM_001312660.2:c.34A>T NP_001299589.1:p.Ile12Phe
NM_001363703.2:c.202A>T NP_001350632.1:p.Ile68Phe
NM_145871.3:c.199A>T NP_665878.2:p.Ile67Phe