Canonical Allele Identifier: CA2737887329

Gene: TXNRD2

Linked Data

• dbSNP Id: rs1555913143

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19919255_19919256insCGCGATCC , CM000684.2:g.19919255_19919256insCGCGATCC	GRCh38
NC_000022.10:g.19906778_19906779insCGCGATCC , CM000684.1:g.19906778_19906779insCGCGATCC	GRCh37
NC_000022.9:g.18286778_18286779insCGCGATCC	NCBI36
NG_011835.1:g.27581_27582insGGATCGCG , LRG_417:g.27581_27582insGGATCGCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.230-252_230-251insGGATCGCG MANE Select	ENSP00000383365.1:n.230-252_230-251insGGATCGCG
ENST00000334363.14:c.230-252_230-251insGGATCGCG	ENSP00000334451.9:n.230-252_230-251insGGATCGCG
ENST00000400518.5:c.140-252_140-251insGGATCGCG	ENSP00000383362.1:n.140-252_140-251insGGATCGCG
ENST00000400519.6:c.227-252_227-251insGGATCGCG	ENSP00000383363.1:n.227-252_227-251insGGATCGCG
ENST00000400521.6:c.230-252_230-251insGGATCGCG	ENSP00000383365.1:n.230-252_230-251insGGATCGCG
ENST00000400525.6:c.161-252_161-251insGGATCGCG	ENSP00000383369.3:n.161-252_161-251insGGATCGCG
ENST00000474308.5:c.173-252_173-251insGGATCGCG	ENSP00000485665.1:n.173-252_173-251insGGATCGCG
ENST00000491939.6:c.134-252_134-251insGGATCGCG	ENSP00000485543.1:n.134-252_134-251insGGATCGCG
ENST00000496729.2:n.235-252_235-251insGGATCGCG
ENST00000542719.6:c.-59-252_-59-251insGGATCGCG	ENSP00000485128.2:n.-59-252_-59-251insGGATCGCG
NM_001282512.1:c.230-252_230-251insGGATCGCG	NP_001269441.1:n.230-252_230-251insGGATCGCG
NM_006440.4:c.230-252_230-251insGGATCGCG	NP_006431.2:n.230-252_230-251insGGATCGCG
NM_001282512.2:c.230-252_230-251insGGATCGCG	NP_001269441.1:n.230-252_230-251insGGATCGCG
NM_001352300.1:c.227-252_227-251insGGATCGCG	NP_001339229.1:n.227-252_227-251insGGATCGCG
NM_001352301.1:c.140-252_140-251insGGATCGCG	NP_001339230.1:n.140-252_140-251insGGATCGCG
NM_001352302.1:c.-59-252_-59-251insGGATCGCG	NP_001339231.1:n.-59-252_-59-251insGGATCGCG
NM_001352303.1:c.134-252_134-251insGGATCGCG	NP_001339232.1:n.134-252_134-251insGGATCGCG
NR_147957.1:n.362-252_362-251insGGATCGCG
NM_006440.5:c.230-252_230-251insGGATCGCG MANE Select	NP_006431.2:n.230-252_230-251insGGATCGCG
NM_001282512.3:c.230-252_230-251insGGATCGCG	NP_001269441.1:n.230-252_230-251insGGATCGCG
NM_001352300.2:c.227-252_227-251insGGATCGCG	NP_001339229.1:n.227-252_227-251insGGATCGCG
NR_147957.2:n.188-252_188-251insGGATCGCG
NM_001352301.2:c.140-252_140-251insGGATCGCG	NP_001339230.1:n.140-252_140-251insGGATCGCG
NM_001352302.2:c.-59-252_-59-251insGGATCGCG	NP_001339231.1:n.-59-252_-59-251insGGATCGCG
NM_001352303.2:c.134-252_134-251insGGATCGCG	NP_001339232.1:n.134-252_134-251insGGATCGCG