Canonical Allele Identifier: CA2588207965

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106784-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106784C>T , CM000681.2:g.1106784C>T	GRCh38
NC_000019.9:g.1106783C>T , CM000681.1:g.1106783C>T	GRCh37
NC_000019.8:g.1057783C>T	NCBI36
NG_050621.1:g.7859C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354171.12:c.*212C>T	ENSP00000346103.7:n.*212C>T
ENST00000588919.5:c.*18C>T	ENSP00000464989.3:n.*18C>T
ENST00000592940.2:n.1177C>T
ENST00000616066.4:c.*212C>T	ENSP00000485000.1:n.*212C>T
ENST00000622390.4:c.*212C>T	ENSP00000477503.1:n.*212C>T
NM_001039847.2:c.*144C>T	NP_001034936.1:n.*144C>T
NM_001039848.2:c.*212C>T	NP_001034937.1:n.*212C>T
NM_002085.4:c.*212C>T	NP_002076.2:n.*212C>T
NM_001039848.3:c.*212C>T	NP_001034937.1:n.*212C>T