Canonical Allele Identifier: CA631298703

Gene: GPX4

Linked Data

• dbSNP Id: rs759367637
• gnomAD v2: 19-1106534-G-C
• gnomAD v3: 19-1106535-G-C
• gnomAD v4: 19-1106535-G-C
• MyVariant Identifiers: chr19:g.1106534G>C (hg19) ; chr19:g.1106535G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106535G>C , CM000681.2:g.1106535G>C	GRCh38
NC_000019.9:g.1106534G>C , CM000681.1:g.1106534G>C	GRCh37
NC_000019.8:g.1057534G>C	NCBI36
NG_050621.1:g.7610G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000585362.7:c.673-5G>C	ENSP00000473614.3:n.673-5G>C
ENST00000593032.6:c.542-5G>C	ENSP00000465828.4:n.542-5G>C
ENST00000706713.1:c.556-5G>C	ENSP00000516510.1:n.556-5G>C
ENST00000706714.1:c.542-5G>C	ENSP00000516511.1:n.542-5G>C
ENST00000706715.1:c.178-5G>C	ENSP00000516512.1:n.178-5G>C
ENST00000354171.13:c.562-5G>C MANE Select	ENSP00000346103.7:n.562-5G>C
ENST00000589115.6:c.537-5G>C	ENSP00000466872.3:n.537-5G>C
ENST00000354171.12:c.562-5G>C	ENSP00000346103.7:n.562-5G>C
ENST00000585480.1:c.295-38G>C	ENSP00000467900.1:n.295-38G>C
ENST00000587648.5:c.442-5G>C	ENSP00000468349.1:n.442-5G>C
ENST00000588919.5:c.503-5G>C	ENSP00000464989.3:n.503-5G>C
ENST00000589115.5:c.537-5G>C	ENSP00000466872.2:n.537-5G>C
ENST00000592940.2:n.933-5G>C
ENST00000611653.4:c.481-5G>C	ENSP00000483655.1:n.481-5G>C
ENST00000616066.4:c.559-5G>C	ENSP00000485000.1:n.559-5G>C
ENST00000622390.4:c.670-5G>C	ENSP00000477503.1:n.670-5G>C
NM_001039847.2:c.584-5G>C	NP_001034936.1:n.584-5G>C
NM_001039848.2:c.673-5G>C	NP_001034937.1:n.673-5G>C
NM_002085.4:c.562-5G>C	NP_002076.2:n.562-5G>C
NM_001039848.3:c.673-5G>C	NP_001034937.1:n.673-5G>C
NM_001039847.3:c.584-5G>C	NP_001034936.1:n.584-5G>C
NM_001039848.4:c.673-5G>C	NP_001034937.1:n.673-5G>C
NM_001367832.1:c.481-5G>C	NP_001354761.1:n.481-5G>C
NM_002085.5:c.562-5G>C MANE Select	NP_002076.2:n.562-5G>C