Canonical Allele Identifier: CA2396084493

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19879970_19879995delinsTAAGCCCAGTCACCCCAAGGCTGCCA , CM000684.2:g.19879970_19879995delinsTAAGCCCAGTCACCCCAAGGCTGCCA	GRCh38
NC_000022.10:g.19867493_19867518delinsTAAGCCCAGTCACCCCAAGGCTGCCA , CM000684.1:g.19867493_19867518delinsTAAGCCCAGTCACCCCAAGGCTGCCA	GRCh37
NC_000022.9:g.18247493_18247518delinsTAAGCCCAGTCACCCCAAGGCTGCCA	NCBI36
NG_011835.1:g.66842_66867delinsTGGCAGCCTTGGGGTGACTGGGCTTA , LRG_417:g.66842_66867delinsTGGCAGCCTTGGGGTGACTGGGCTTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.1275+184_1275+209delinsTGGCAGCCTTGGGGTGACTGGGCTTA MANE Select	ENSP00000383365.1:n.1275+184_1275+209delinsTGGCAGCCTTGGGGTGAC...
ENST00000400518.5:c.1185+184_1185+209delinsTGGCAGCCTTGGGGTGACTGGGCTTA	ENSP00000383362.1:n.1185+184_1185+209delinsTGGCAGCCTTGGGGTGAC...
ENST00000400519.6:c.1272+184_1272+209delinsTGGCAGCCTTGGGGTGACTGGGCTTA	ENSP00000383363.1:n.1272+184_1272+209delinsTGGCAGCCTTGGGGTGAC...
ENST00000400521.6:c.1275+184_1275+209delinsTGGCAGCCTTGGGGTGACTGGGCTTA	ENSP00000383365.1:n.1275+184_1275+209delinsTGGCAGCCTTGGGGTGAC...
ENST00000400525.6:c.1206+184_1206+209delinsTGGCAGCCTTGGGGTGACTGGGCTTA	ENSP00000383369.3:n.1206+184_1206+209delinsTGGCAGCCTTGGGGTGAC...
ENST00000462330.5:c.198+184_198+209delinsTGGCAGCCTTGGGGTGACTGGGCTTA	ENSP00000485603.2:n.198+184_198+209delinsTGGCAGCCTTGGGGTGACTG...
ENST00000462843.2:c.225+184_225+209delinsTGGCAGCCTTGGGGTGACTGGGCTTA	ENSP00000485466.2:n.225+184_225+209delinsTGGCAGCCTTGGGGTGACTG...
ENST00000474308.5:c.1218+184_1218+209delinsTGGCAGCCTTGGGGTGACTGGGCTTA	ENSP00000485665.1:n.1218+184_1218+209delinsTGGCAGCCTTGGGGTGAC...
ENST00000485358.5:c.243+184_243+209delinsTGGCAGCCTTGGGGTGACTGGGCTTA	ENSP00000485499.2:n.243+184_243+209delinsTGGCAGCCTTGGGGTGACTG...
ENST00000487165.5:n.1369+184_1369+209delinsTGGCAGCCTTGGGGTGACTGGGCTTA
ENST00000494454.5:n.1349+184_1349+209delinsTGGCAGCCTTGGGGTGACTGGGCTTA
ENST00000495655.2:n.819+184_819+209delinsTGGCAGCCTTGGGGTGACTGGGCTTA
ENST00000542719.6:c.987+184_987+209delinsTGGCAGCCTTGGGGTGACTGGGCTTA	ENSP00000485128.2:n.987+184_987+209delinsTGGCAGCCTTGGGGTGACTG...
ENST00000634471.1:n.336+184_336+209delinsTGGCAGCCTTGGGGTGACTGGGCTTA
ENST00000634537.1:c.504+184_504+209delinsTGGCAGCCTTGGGGTGACTGGGCTTA	ENSP00000489208.1:n.504+184_504+209delinsTGGCAGCCTTGGGGTGACTG...
NM_006440.4:c.1275+184_1275+209delinsTGGCAGCCTTGGGGTGACTGGGCTTA	NP_006431.2:n.1275+184_1275+209delinsTGGCAGCCTTGGGGTGACTGGGCT...
NM_001352300.1:c.1272+184_1272+209delinsTGGCAGCCTTGGGGTGACTGGGCTTA	NP_001339229.1:n.1272+184_1272+209delinsTGGCAGCCTTGGGGTGACTGG...
NM_001352301.1:c.1185+184_1185+209delinsTGGCAGCCTTGGGGTGACTGGGCTTA	NP_001339230.1:n.1185+184_1185+209delinsTGGCAGCCTTGGGGTGACTGG...
NM_001352302.1:c.987+184_987+209delinsTGGCAGCCTTGGGGTGACTGGGCTTA	NP_001339231.1:n.987+184_987+209delinsTGGCAGCCTTGGGGTGACTGGGC...
NR_147957.1:n.1407+184_1407+209delinsTGGCAGCCTTGGGGTGACTGGGCTTA
NM_006440.5:c.1275+184_1275+209delinsTGGCAGCCTTGGGGTGACTGGGCTTA MANE Select	NP_006431.2:n.1275+184_1275+209delinsTGGCAGCCTTGGGGTGACTGGGCT...
NM_001352300.2:c.1272+184_1272+209delinsTGGCAGCCTTGGGGTGACTGGGCTTA	NP_001339229.1:n.1272+184_1272+209delinsTGGCAGCCTTGGGGTGACTGG...
NR_147957.2:n.1233+184_1233+209delinsTGGCAGCCTTGGGGTGACTGGGCTTA
NM_001352301.2:c.1185+184_1185+209delinsTGGCAGCCTTGGGGTGACTGGGCTTA	NP_001339230.1:n.1185+184_1185+209delinsTGGCAGCCTTGGGGTGACTGG...
NM_001352302.2:c.987+184_987+209delinsTGGCAGCCTTGGGGTGACTGGGCTTA	NP_001339231.1:n.987+184_987+209delinsTGGCAGCCTTGGGGTGACTGGGC...