Canonical Allele Identifier: CA352783329

Gene: GPX1

Linked Data

• dbSNP Id: rs1207819543
• gnomAD v2: 3-49395560-G-T
• gnomAD v4: 3-49358127-G-T
• MyVariant Identifiers: chr3:g.49395560G>T (hg19) ; chr3:g.49358127G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49358127G>T , CM000665.2:g.49358127G>T	GRCh38
NC_000003.11:g.49395560G>T , CM000665.1:g.49395560G>T	GRCh37
NC_000003.10:g.49370564G>T	NCBI36
NG_012264.1:g.5232C>A
NG_051308.1:g.58971C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419349.3:c.152C>A	ENSP00000391316.1:p.Thr51Asn
ENST00000496791.3:c.152C>A	ENSP00000493593.2:p.Thr51Asn
ENST00000643797.2:c.114+38C>A	ENSP00000495108.1:n.114+38C>A
ENST00000646881.3:c.152C>A	ENSP00000495001.2:p.Thr51Asn
ENST00000703795.1:c.152C>A	ENSP00000515480.1:p.Thr51Asn
ENST00000703796.1:c.152C>A	ENSP00000515481.1:p.Thr51Asn
ENST00000703797.1:c.152C>A	ENSP00000515482.1:p.Thr51Asn
ENST00000704356.1:c.152C>A	ENSP00000515867.1:p.Thr51Asn
ENST00000704374.1:c.87+65C>A	ENSP00000515879.1:n.87+65C>A
ENST00000704375.1:c.152C>A	ENSP00000515880.1:p.Thr51Asn
ENST00000704376.1:c.148+4C>A	ENSP00000515881.1:n.148+4C>A
ENST00000704377.1:c.114+38C>A	ENSP00000515882.1:n.114+38C>A
ENST00000704378.1:c.152C>A	ENSP00000515883.1:p.Thr51Asn
ENST00000704379.1:n.126-380C>A
ENST00000704380.1:n.86-380C>A
ENST00000704381.1:c.465-380C>A	ENSP00000515884.1:n.465-380C>A
ENST00000419349.2:c.152C>A	ENSP00000391316.1:p.Thr51Asn
ENST00000419783.3:c.152C>A MANE Select	ENSP00000407375.1:p.Thr51Asn
ENST00000496791.2:c.152C>A	ENSP00000493593.2:p.Thr51Asn
ENST00000643797.1:c.114+38C>A	ENSP00000495108.1:n.114+38C>A
ENST00000646881.2:c.152C>A	ENSP00000495001.2:p.Thr51Asn
ENST00000419349.1:c.152C>A	ENSP00000391316.1:p.Thr51Asn
ENST00000419783.1:c.152C>A	ENSP00000407375.1:p.Thr51Asn
ENST00000496791.1:n.199C>A
ENST00000620890.1:c.149C>A	ENSP00000478837.1:p.Thr50Asn
NM_000581.2:c.152C>A	NP_000572.2:p.Thr51Asn
NM_201397.1:c.152C>A	NP_958799.1:p.Thr51Asn
NM_000581.3:c.152C>A	NP_000572.2:p.Thr51Asn
NM_001329455.1:c.114+38C>A	NP_001316384.1:n.114+38C>A
NM_001329502.1:c.152C>A	NP_001316431.1:p.Thr51Asn
NM_001329503.1:c.152C>A	NP_001316432.1:p.Thr51Asn
NM_201397.2:c.152C>A	NP_958799.1:p.Thr51Asn
NM_000581.4:c.152C>A MANE Select	NP_000572.2:p.Thr51Asn
NM_001329502.2:c.152C>A	NP_001316431.1:p.Thr51Asn
NM_001329503.2:c.152C>A	NP_001316432.1:p.Thr51Asn
NM_201397.3:c.152C>A	NP_958799.1:p.Thr51Asn
NM_001329455.2:c.114+38C>A	NP_001316384.1:n.114+38C>A