Canonical Allele Identifier: CA2509236627

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918976_19918977insAGGGCGACCTTCTTGCCCGCGTGTCCGAGGCGCTCGGCGGC , CM000684.2:g.19918976_19918977insAGGGCGACCTTCTTGCCCGCGTGTCCGAGGCGCTCGGCGGC	GRCh38
NC_000022.10:g.19906499_19906500insAGGGCGACCTTCTTGCCCGCGTGTCCGAGGCGCTCGGCGGC , CM000684.1:g.19906499_19906500insAGGGCGACCTTCTTGCCCGCGTGTCCGAGGCGCTCGGCGGC	GRCh37
NC_000022.9:g.18286499_18286500insAGGGCGACCTTCTTGCCCGCGTGTCCGAGGCGCTCGGCGGC	NCBI36
NG_011835.1:g.27860_27861insGCCGCCGAGCGCCTCGGACACGCGGGCAAGAAGGTCGCCCT , LRG_417:g.27860_27861insGCCGCCGAGCGCCTCGGACACGCGGGCAAGAAGGTCGCCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.257_258insGCCGCCGAGCGCCTCGGACACGCGGGCAAGAAGGTCGCCCT MANE Select	ENSP00000383365.1:p.Cys86TrpfsTer25
ENST00000334363.14:c.257_258insGCCGCCGAGCGCCTCGGACACGCGGGCAAGAAGGTCGCCCT	ENSP00000334451.9:p.Cys86TrpfsTer25
ENST00000400518.5:c.167_168insGCCGCCGAGCGCCTCGGACACGCGGGCAAGAAGGTCGCCCT	ENSP00000383362.1:p.Cys56TrpfsTer25
ENST00000400519.6:c.254_255insGCCGCCGAGCGCCTCGGACACGCGGGCAAGAAGGTCGCCCT	ENSP00000383363.1:p.Cys85TrpfsTer25
ENST00000400521.6:c.257_258insGCCGCCGAGCGCCTCGGACACGCGGGCAAGAAGGTCGCCCT	ENSP00000383365.1:p.Cys86TrpfsTer25
ENST00000400525.6:c.188_189insGCCGCCGAGCGCCTCGGACACGCGGGCAAGAAGGTCGCCCT	ENSP00000383369.3:p.Cys63TrpfsTer25
ENST00000474308.5:c.200_201insGCCGCCGAGCGCCTCGGACACGCGGGCAAGAAGGTCGCCCT	ENSP00000485665.1:p.Cys67TrpfsTer25
ENST00000491939.6:c.161_162insGCCGCCGAGCGCCTCGGACACGCGGGCAAGAAGGTCGCCCT	ENSP00000485543.1:p.Cys54TrpfsTer25
ENST00000496729.2:n.262_263insGCCGCCGAGCGCCTCGGACACGCGGGCAAGAAGGTCGCCCT
ENST00000542719.6:c.-32_-31insGCCGCCGAGCGCCTCGGACACGCGGGCAAGAAGGTCGCCCT	ENSP00000485128.2:n.-32_-31insGCCGCCGAGCGCCTCGGACACGCGGGCAAGA...
NM_001282512.1:c.257_258insGCCGCCGAGCGCCTCGGACACGCGGGCAAGAAGGTCGCCCT	NP_001269441.1:p.Cys86TrpfsTer25
NM_006440.4:c.257_258insGCCGCCGAGCGCCTCGGACACGCGGGCAAGAAGGTCGCCCT	NP_006431.2:p.Cys86TrpfsTer25
NM_001282512.2:c.257_258insGCCGCCGAGCGCCTCGGACACGCGGGCAAGAAGGTCGCCCT	NP_001269441.1:p.Cys86TrpfsTer25
NM_001352300.1:c.254_255insGCCGCCGAGCGCCTCGGACACGCGGGCAAGAAGGTCGCCCT	NP_001339229.1:p.Cys85TrpfsTer25
NM_001352301.1:c.167_168insGCCGCCGAGCGCCTCGGACACGCGGGCAAGAAGGTCGCCCT	NP_001339230.1:p.Cys56TrpfsTer25
NM_001352302.1:c.-32_-31insGCCGCCGAGCGCCTCGGACACGCGGGCAAGAAGGTCGCCCT	NP_001339231.1:n.-32_-31insGCCGCCGAGCGCCTCGGACACGCGGGCAAGAAGG...
NM_001352303.1:c.161_162insGCCGCCGAGCGCCTCGGACACGCGGGCAAGAAGGTCGCCCT	NP_001339232.1:p.Cys54TrpfsTer25
NR_147957.1:n.389_390insGCCGCCGAGCGCCTCGGACACGCGGGCAAGAAGGTCGCCCT
NM_006440.5:c.257_258insGCCGCCGAGCGCCTCGGACACGCGGGCAAGAAGGTCGCCCT MANE Select	NP_006431.2:p.Cys86TrpfsTer25
NM_001282512.3:c.257_258insGCCGCCGAGCGCCTCGGACACGCGGGCAAGAAGGTCGCCCT	NP_001269441.1:p.Cys86TrpfsTer25
NM_001352300.2:c.254_255insGCCGCCGAGCGCCTCGGACACGCGGGCAAGAAGGTCGCCCT	NP_001339229.1:p.Cys85TrpfsTer25
NR_147957.2:n.215_216insGCCGCCGAGCGCCTCGGACACGCGGGCAAGAAGGTCGCCCT
NM_001352301.2:c.167_168insGCCGCCGAGCGCCTCGGACACGCGGGCAAGAAGGTCGCCCT	NP_001339230.1:p.Cys56TrpfsTer25
NM_001352302.2:c.-32_-31insGCCGCCGAGCGCCTCGGACACGCGGGCAAGAAGGTCGCCCT	NP_001339231.1:n.-32_-31insGCCGCCGAGCGCCTCGGACACGCGGGCAAGAAGG...
NM_001352303.2:c.161_162insGCCGCCGAGCGCCTCGGACACGCGGGCAAGAAGGTCGCCCT	NP_001339232.1:p.Cys54TrpfsTer25