Canonical Allele Identifier: CA2588207101

Gene: GPX4

Linked Data

• gnomAD v4: 19-1105562-G-GGCCCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105562_1105563insGCCCCCC , CM000681.2:g.1105562_1105563insGCCCCCC	GRCh38
NC_000019.9:g.1105561_1105562insGCCCCCC , CM000681.1:g.1105561_1105562insGCCCCCC	GRCh37
NC_000019.8:g.1056561_1056562insGCCCCCC	NCBI36
NG_050621.1:g.6637_6638insGCCCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.435+52_435+53insGCCCCCC	ENSP00000473614.3:n.435+52_435+53insGCCCCCC
ENST00000593032.6:c.243+52_243+53insGCCCCCC	ENSP00000465828.4:n.243+52_243+53insGCCCCCC
ENST00000706713.1:c.318+52_318+53insGCCCCCC	ENSP00000516510.1:n.318+52_318+53insGCCCCCC
ENST00000706714.1:c.243+52_243+53insGCCCCCC	ENSP00000516511.1:n.243+52_243+53insGCCCCCC
ENST00000706715.1:c.-61+52_-61+53insGCCCCCC	ENSP00000516512.1:n.-61+52_-61+53insGCCCCCC
ENST00000354171.13:c.324+52_324+53insGCCCCCC MANE Select	ENSP00000346103.7:n.324+52_324+53insGCCCCCC
ENST00000589115.6:c.324+52_324+53insGCCCCCC	ENSP00000466872.3:n.324+52_324+53insGCCCCCC
ENST00000354171.12:c.324+52_324+53insGCCCCCC	ENSP00000346103.7:n.324+52_324+53insGCCCCCC
ENST00000585362.6:c.435+52_435+53insGCCCCCC	ENSP00000473614.2:n.435+52_435+53insGCCCCCC
ENST00000585480.1:c.57+52_57+53insGCCCCCC	ENSP00000467900.1:n.57+52_57+53insGCCCCCC
ENST00000587648.5:c.204+52_204+53insGCCCCCC	ENSP00000468349.1:n.204+52_204+53insGCCCCCC
ENST00000587932.2:n.258+52_258+53insGCCCCCC
ENST00000588919.5:c.243+52_243+53insGCCCCCC	ENSP00000464989.3:n.243+52_243+53insGCCCCCC
ENST00000589115.5:c.324+52_324+53insGCCCCCC	ENSP00000466872.2:n.324+52_324+53insGCCCCCC
ENST00000592940.2:n.270+52_270+53insGCCCCCC
ENST00000593032.5:c.243+52_243+53insGCCCCCC	ENSP00000465828.3:n.243+52_243+53insGCCCCCC
ENST00000611653.4:c.243+52_243+53insGCCCCCC	ENSP00000483655.1:n.243+52_243+53insGCCCCCC
ENST00000616066.4:c.321+52_321+53insGCCCCCC	ENSP00000485000.1:n.321+52_321+53insGCCCCCC
ENST00000622390.4:c.432+52_432+53insGCCCCCC	ENSP00000477503.1:n.432+52_432+53insGCCCCCC
NM_001039847.2:c.324+52_324+53insGCCCCCC	NP_001034936.1:n.324+52_324+53insGCCCCCC
NM_001039848.2:c.435+52_435+53insGCCCCCC	NP_001034937.1:n.435+52_435+53insGCCCCCC
NM_002085.4:c.324+52_324+53insGCCCCCC	NP_002076.2:n.324+52_324+53insGCCCCCC
NM_001039848.3:c.435+52_435+53insGCCCCCC	NP_001034937.1:n.435+52_435+53insGCCCCCC
NM_001039847.3:c.324+52_324+53insGCCCCCC	NP_001034936.1:n.324+52_324+53insGCCCCCC
NM_001039848.4:c.435+52_435+53insGCCCCCC	NP_001034937.1:n.435+52_435+53insGCCCCCC
NM_001367832.1:c.243+52_243+53insGCCCCCC	NP_001354761.1:n.243+52_243+53insGCCCCCC
NM_002085.5:c.324+52_324+53insGCCCCCC MANE Select	NP_002076.2:n.324+52_324+53insGCCCCCC