Canonical Allele Identifier: CA2588205784

Gene: GPX4

Linked Data

• gnomAD v4: 19-1104009-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1104009G>T , CM000681.2:g.1104009G>T	GRCh38
NC_000019.9:g.1104008G>T , CM000681.1:g.1104008G>T	GRCh37
NC_000019.8:g.1055008G>T	NCBI36
NG_050621.1:g.5084G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706713.1:c.-35G>T	ENSP00000516510.1:n.-35G>T
ENST00000354171.13:c.-35G>T MANE Select	ENSP00000346103.7:n.-35G>T
ENST00000589115.6:c.-35G>T	ENSP00000466872.3:n.-35G>T
ENST00000354171.12:c.-35G>T	ENSP00000346103.7:n.-35G>T
ENST00000589115.5:c.-35G>T	ENSP00000466872.2:n.-35G>T
ENST00000616066.4:c.-35G>T	ENSP00000485000.1:n.-35G>T
NM_001039847.2:c.-35G>T	NP_001034936.1:n.-35G>T
NM_002085.4:c.-35G>T	NP_002076.2:n.-35G>T
NM_001039847.3:c.-35G>T	NP_001034936.1:n.-35G>T
NM_002085.5:c.-35G>T MANE Select	NP_002076.2:n.-35G>T