Canonical Allele Identifier: CA2573157745

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880694_19880695delinsCG , CM000684.2:g.19880694_19880695delinsCG	GRCh38
NC_000022.10:g.19868217_19868218delinsCG , CM000684.1:g.19868217_19868218delinsCG	GRCh37
NC_000022.9:g.18248217_18248218delinsCG	NCBI36
NG_011835.1:g.66142_66143delinsCG , LRG_417:g.66142_66143delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1109_1110delinsCG MANE Select	ENSP00000383365.1:p.Ile370Thr
ENST00000400518.5:c.1019_1020delinsCG	ENSP00000383362.1:p.Ile340Thr
ENST00000400519.6:c.1106_1107delinsCG	ENSP00000383363.1:p.Ile369Thr
ENST00000400521.6:c.1109_1110delinsCG	ENSP00000383365.1:p.Ile370Thr
ENST00000400525.6:c.1040_1041delinsCG	ENSP00000383369.3:p.Ile347Thr
ENST00000462330.5:c.32_33delinsCG	ENSP00000485603.2:p.Ile11Thr
ENST00000462843.2:c.59_60delinsCG	ENSP00000485466.2:p.Ile20Thr
ENST00000474308.5:c.1052_1053delinsCG	ENSP00000485665.1:p.Ile351Thr
ENST00000485358.5:c.77_78delinsCG	ENSP00000485499.2:p.Ile26Thr
ENST00000487165.5:n.1203_1204delinsCG
ENST00000494454.5:n.1183_1184delinsCG
ENST00000495655.2:n.653_654delinsCG
ENST00000542719.6:c.821_822delinsCG	ENSP00000485128.2:p.Ile274Thr
ENST00000634471.1:n.244-424_244-423delinsCG
ENST00000634537.1:c.338_339delinsCG	ENSP00000489208.1:p.Ile113Thr
NM_006440.4:c.1109_1110delinsCG	NP_006431.2:p.Ile370Thr
NM_001352300.1:c.1106_1107delinsCG	NP_001339229.1:p.Ile369Thr
NM_001352301.1:c.1019_1020delinsCG	NP_001339230.1:p.Ile340Thr
NM_001352302.1:c.821_822delinsCG	NP_001339231.1:p.Ile274Thr
NR_147957.1:n.1241_1242delinsCG
NM_006440.5:c.1109_1110delinsCG MANE Select	NP_006431.2:p.Ile370Thr
NM_001352300.2:c.1106_1107delinsCG	NP_001339229.1:p.Ile369Thr
NR_147957.2:n.1067_1068delinsCG
NM_001352301.2:c.1019_1020delinsCG	NP_001339230.1:p.Ile340Thr
NM_001352302.2:c.821_822delinsCG	NP_001339231.1:p.Ile274Thr