Canonical Allele Identifier: CA2676036195

Gene: GPX3

Linked Data

• gnomAD v4: 5-151028382-T-TCTAC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151028386_151028389dup , CM000667.2:g.151028386_151028389dup	GRCh38
NC_000005.9:g.150407947_150407950dup , CM000667.1:g.150407947_150407950dup	GRCh37
NC_000005.8:g.150388140_150388143dup	NCBI36
NG_030590.1:g.64275_64278dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388825.9:c.*256_*259dup MANE Select	ENSP00000373477.4:n.*256_*259dup
ENST00000388825.8:c.*256_*259dup	ENSP00000373477.4:n.*256_*259dup
ENST00000521632.1:c.746_749dup
ENST00000614343.4:c.*718_*721dup	ENSP00000483660.1:n.*718_*721dup
ENST00000622181.4:c.*256_*259dup	ENSP00000484258.1:n.*256_*259dup
NM_002084.3:c.*256_*259dup	NP_002075.2:n.*256_*259dup
NM_001329790.1:c.*256_*259dup	NP_001316719.1:n.*256_*259dup
NM_002084.4:c.*256_*259dup	NP_002075.2:n.*256_*259dup
NM_002084.5:c.*256_*259dup MANE Select	NP_002075.2:n.*256_*259dup
NM_001329790.2:c.*256_*259dup	NP_001316719.1:n.*256_*259dup