Canonical Allele Identifier: CA2396103794

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918989_19918990delinsAG , CM000684.2:g.19918989_19918990delinsAG	GRCh38
NC_000022.10:g.19906512_19906513delinsAG , CM000684.1:g.19906512_19906513delinsAG	GRCh37
NC_000022.9:g.18286512_18286513delinsAG	NCBI36
NG_011835.1:g.27847_27848delinsCT , LRG_417:g.27847_27848delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.244_245delinsCT MANE Select	ENSP00000383365.1:p.Leu82=
ENST00000334363.14:c.244_245delinsCT	ENSP00000334451.9:p.Leu82=
ENST00000400518.5:c.154_155delinsCT	ENSP00000383362.1:p.Leu52=
ENST00000400519.6:c.241_242delinsCT	ENSP00000383363.1:p.Leu81=
ENST00000400521.6:c.244_245delinsCT	ENSP00000383365.1:p.Leu82=
ENST00000400525.6:c.175_176delinsCT	ENSP00000383369.3:p.Leu59=
ENST00000474308.5:c.187_188delinsCT	ENSP00000485665.1:p.Leu63=
ENST00000491939.6:c.148_149delinsCT	ENSP00000485543.1:p.Leu50=
ENST00000496729.2:n.249_250delinsCT
ENST00000542719.6:c.-45_-44delinsCT	ENSP00000485128.2:n.-45_-44delinsCT
NM_001282512.1:c.244_245delinsCT	NP_001269441.1:p.Leu82=
NM_006440.4:c.244_245delinsCT	NP_006431.2:p.Leu82=
NM_001282512.2:c.244_245delinsCT	NP_001269441.1:p.Leu82=
NM_001352300.1:c.241_242delinsCT	NP_001339229.1:p.Leu81=
NM_001352301.1:c.154_155delinsCT	NP_001339230.1:p.Leu52=
NM_001352302.1:c.-45_-44delinsCT	NP_001339231.1:n.-45_-44delinsCT
NM_001352303.1:c.148_149delinsCT	NP_001339232.1:p.Leu50=
NR_147957.1:n.376_377delinsCT
NM_006440.5:c.244_245delinsCT MANE Select	NP_006431.2:p.Leu82=
NM_001282512.3:c.244_245delinsCT	NP_001269441.1:p.Leu82=
NM_001352300.2:c.241_242delinsCT	NP_001339229.1:p.Leu81=
NR_147957.2:n.202_203delinsCT
NM_001352301.2:c.154_155delinsCT	NP_001339230.1:p.Leu52=
NM_001352302.2:c.-45_-44delinsCT	NP_001339231.1:n.-45_-44delinsCT
NM_001352303.2:c.148_149delinsCT	NP_001339232.1:p.Leu50=