Canonical Allele Identifier: CA381521762

Gene: GSTP1

Linked Data

• gnomAD v4: 11-67586224-C-T
• MyVariant Identifiers: chr11:g.67353695C>T (hg19) ; chr11:g.67586224C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586224C>T , CM000673.2:g.67586224C>T	GRCh38
NC_000011.9:g.67353695C>T , CM000673.1:g.67353695C>T	GRCh37
NC_000011.8:g.67110271C>T	NCBI36
NG_012075.1:g.7630C>T , LRG_723:g.7630C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.337-165C>T	ENSP00000381604.1:n.337-165C>T
ENST00000398606.10:c.444+13C>T MANE Select	ENSP00000381607.3:n.444+13C>T
ENST00000646888.1:c.*160+13C>T	ENSP00000494477.1:n.*160+13C>T
ENST00000398603.5:c.337-165C>T	ENSP00000381604.1:n.337-165C>T
ENST00000398606.7:c.444+13C>T	ENSP00000381607.3:n.444+13C>T
ENST00000467591.1:n.555+13C>T
ENST00000494593.1:n.1252C>T
ENST00000495996.1:c.121C>T	ENSP00000484686.1:p.Pro41Ser
ENST00000498765.5:c.507+13C>T
NM_000852.3:c.444+13C>T , LRG_723t1:c.444+13C>T	NP_000843.1:n.444+13C>T
NM_000852.4:c.444+13C>T MANE Select	NP_000843.1:n.444+13C>T