Canonical Allele Identifier: CA2396114626

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19940636_19940637delinsCT , CM000684.2:g.19940636_19940637delinsCT	GRCh38
NC_000022.10:g.19928159_19928160delinsCT , CM000684.1:g.19928159_19928160delinsCT	GRCh37
NC_000022.9:g.18308159_18308160delinsCT	NCBI36
NG_011526.1:g.3897_3898delinsCT
NG_011835.1:g.6200_6201delinsAG , LRG_417:g.6200_6201delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.103+1064_103+1065delinsAG MANE Select	ENSP00000383365.1:n.103+1064_103+1065delinsAG
ENST00000334363.14:c.103+1064_103+1065delinsAG	ENSP00000334451.9:n.103+1064_103+1065delinsAG
ENST00000400519.6:c.103+1064_103+1065delinsAG	ENSP00000383363.1:n.103+1064_103+1065delinsAG
ENST00000400521.6:c.103+1064_103+1065delinsAG	ENSP00000383365.1:n.103+1064_103+1065delinsAG
ENST00000400525.6:c.103+1064_103+1065delinsAG	ENSP00000383369.3:n.103+1064_103+1065delinsAG
ENST00000474308.5:c.103+1064_103+1065delinsAG	ENSP00000485665.1:n.103+1064_103+1065delinsAG
ENST00000496729.2:n.108+1064_108+1065delinsAG
NM_001282512.1:c.103+1064_103+1065delinsAG	NP_001269441.1:n.103+1064_103+1065delinsAG
NM_006440.4:c.103+1064_103+1065delinsAG	NP_006431.2:n.103+1064_103+1065delinsAG
NM_001282512.2:c.103+1064_103+1065delinsAG	NP_001269441.1:n.103+1064_103+1065delinsAG
NM_001352300.1:c.103+1064_103+1065delinsAG	NP_001339229.1:n.103+1064_103+1065delinsAG
NR_147957.1:n.292+1064_292+1065delinsAG
NM_006440.5:c.103+1064_103+1065delinsAG MANE Select	NP_006431.2:n.103+1064_103+1065delinsAG
NM_001282512.3:c.103+1064_103+1065delinsAG	NP_001269441.1:n.103+1064_103+1065delinsAG
NM_001352300.2:c.103+1064_103+1065delinsAG	NP_001339229.1:n.103+1064_103+1065delinsAG
NR_147957.2:n.118+1064_118+1065delinsAG