Canonical Allele Identifier: CA15389968

Gene: GPX3

Linked Data

• dbSNP Id: rs549115808
• gnomAD v2: 5-150405972-T-C
• gnomAD v3: 5-151026411-T-C
• gnomAD v4: 5-151026411-T-C
• MyVariant Identifiers: chr5:g.150405972T>C (hg19) ; chr5:g.151026411T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151026411T>C , CM000667.2:g.151026411T>C	GRCh38
NC_000005.9:g.150405972T>C , CM000667.1:g.150405972T>C	GRCh37
NC_000005.8:g.150386165T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388825.9:c.242-489T>C MANE Select	ENSP00000373477.4:n.242-489T>C
ENST00000388825.8:c.242-489T>C	ENSP00000373477.4:n.242-489T>C
ENST00000517973.1:c.88-489T>C	ENSP00000429709.1:n.88-489T>C
ENST00000519214.5:c.*476-489T>C	ENSP00000430508.1:n.*476-489T>C
ENST00000521632.1:c.151-489T>C
ENST00000521650.5:c.269-489T>C	ENSP00000427873.1:n.269-489T>C
ENST00000521722.5:n.305-300T>C
ENST00000614343.4:c.*23-489T>C	ENSP00000483660.1:n.*23-489T>C
ENST00000622181.4:c.239-489T>C	ENSP00000484258.1:n.239-489T>C
NM_002084.3:c.242-489T>C	NP_002075.2:n.242-489T>C
NM_001329790.1:c.269-489T>C	NP_001316719.1:n.269-489T>C
NM_002084.4:c.242-489T>C	NP_002075.2:n.242-489T>C
NM_002084.5:c.242-489T>C MANE Select	NP_002075.2:n.242-489T>C
NM_001329790.2:c.269-489T>C	NP_001316719.1:n.269-489T>C