Canonical Allele Identifier: CA2655329234

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19918785-A-AGGCTTATCCTCCATGAGCCCTCATGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918787_19918788insCTTATCCTCCATGAGCCCTCATGGGGG , CM000684.2:g.19918787_19918788insCTTATCCTCCATGAGCCCTCATGGGGG	GRCh38
NC_000022.10:g.19906310_19906311insCTTATCCTCCATGAGCCCTCATGGGGG , CM000684.1:g.19906310_19906311insCTTATCCTCCATGAGCCCTCATGGGGG	GRCh37
NC_000022.9:g.18286310_18286311insCTTATCCTCCATGAGCCCTCATGGGGG	NCBI36
NG_011835.1:g.28051_28052insCCCATGAGGGCTCATGGAGGATAAGCC , LRG_417:g.28051_28052insCCCATGAGGGCTCATGGAGGATAAGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.374+74_374+75insCCCATGAGGGCTCATGGAGGATAAGCC MANE Select	ENSP00000383365.1:n.374+74_374+75insCCCATGAGGGCTCATGGAGGATAAG...
ENST00000334363.14:c.374+74_374+75insCCCATGAGGGCTCATGGAGGATAAGCC	ENSP00000334451.9:n.374+74_374+75insCCCATGAGGGCTCATGGAGGATAAG...
ENST00000400518.5:c.284+74_284+75insCCCATGAGGGCTCATGGAGGATAAGCC	ENSP00000383362.1:n.284+74_284+75insCCCATGAGGGCTCATGGAGGATAAG...
ENST00000400519.6:c.371+74_371+75insCCCATGAGGGCTCATGGAGGATAAGCC	ENSP00000383363.1:n.371+74_371+75insCCCATGAGGGCTCATGGAGGATAAG...
ENST00000400521.6:c.374+74_374+75insCCCATGAGGGCTCATGGAGGATAAGCC	ENSP00000383365.1:n.374+74_374+75insCCCATGAGGGCTCATGGAGGATAAG...
ENST00000400525.6:c.305+74_305+75insCCCATGAGGGCTCATGGAGGATAAGCC	ENSP00000383369.3:n.305+74_305+75insCCCATGAGGGCTCATGGAGGATAAG...
ENST00000474308.5:c.317+74_317+75insCCCATGAGGGCTCATGGAGGATAAGCC	ENSP00000485665.1:n.317+74_317+75insCCCATGAGGGCTCATGGAGGATAAG...
ENST00000491939.6:c.278+74_278+75insCCCATGAGGGCTCATGGAGGATAAGCC	ENSP00000485543.1:n.278+74_278+75insCCCATGAGGGCTCATGGAGGATAAG...
ENST00000496729.2:n.379+74_379+75insCCCATGAGGGCTCATGGAGGATAAGCC
ENST00000542719.6:c.86+74_86+75insCCCATGAGGGCTCATGGAGGATAAGCC	ENSP00000485128.2:n.86+74_86+75insCCCATGAGGGCTCATGGAGGATAAGCC...
NM_001282512.1:c.374+74_374+75insCCCATGAGGGCTCATGGAGGATAAGCC	NP_001269441.1:n.374+74_374+75insCCCATGAGGGCTCATGGAGGATAAGCC
NM_006440.4:c.374+74_374+75insCCCATGAGGGCTCATGGAGGATAAGCC	NP_006431.2:n.374+74_374+75insCCCATGAGGGCTCATGGAGGATAAGCC
NM_001282512.2:c.374+74_374+75insCCCATGAGGGCTCATGGAGGATAAGCC	NP_001269441.1:n.374+74_374+75insCCCATGAGGGCTCATGGAGGATAAGCC
NM_001352300.1:c.371+74_371+75insCCCATGAGGGCTCATGGAGGATAAGCC	NP_001339229.1:n.371+74_371+75insCCCATGAGGGCTCATGGAGGATAAGCC
NM_001352301.1:c.284+74_284+75insCCCATGAGGGCTCATGGAGGATAAGCC	NP_001339230.1:n.284+74_284+75insCCCATGAGGGCTCATGGAGGATAAGCC
NM_001352302.1:c.86+74_86+75insCCCATGAGGGCTCATGGAGGATAAGCC	NP_001339231.1:n.86+74_86+75insCCCATGAGGGCTCATGGAGGATAAGCC
NM_001352303.1:c.278+74_278+75insCCCATGAGGGCTCATGGAGGATAAGCC	NP_001339232.1:n.278+74_278+75insCCCATGAGGGCTCATGGAGGATAAGCC
NR_147957.1:n.506+74_506+75insCCCATGAGGGCTCATGGAGGATAAGCC
NM_006440.5:c.374+74_374+75insCCCATGAGGGCTCATGGAGGATAAGCC MANE Select	NP_006431.2:n.374+74_374+75insCCCATGAGGGCTCATGGAGGATAAGCC
NM_001282512.3:c.374+74_374+75insCCCATGAGGGCTCATGGAGGATAAGCC	NP_001269441.1:n.374+74_374+75insCCCATGAGGGCTCATGGAGGATAAGCC
NM_001352300.2:c.371+74_371+75insCCCATGAGGGCTCATGGAGGATAAGCC	NP_001339229.1:n.371+74_371+75insCCCATGAGGGCTCATGGAGGATAAGCC
NR_147957.2:n.332+74_332+75insCCCATGAGGGCTCATGGAGGATAAGCC
NM_001352301.2:c.284+74_284+75insCCCATGAGGGCTCATGGAGGATAAGCC	NP_001339230.1:n.284+74_284+75insCCCATGAGGGCTCATGGAGGATAAGCC
NM_001352302.2:c.86+74_86+75insCCCATGAGGGCTCATGGAGGATAAGCC	NP_001339231.1:n.86+74_86+75insCCCATGAGGGCTCATGGAGGATAAGCC
NM_001352303.2:c.278+74_278+75insCCCATGAGGGCTCATGGAGGATAAGCC	NP_001339232.1:n.278+74_278+75insCCCATGAGGGCTCATGGAGGATAAGCC