Canonical Allele Identifier: CA751471532

Gene: TXNRD2

Linked Data

• dbSNP Id: rs1172774616
• MyVariant Identifiers: chr22:g.19928507_19928508insG (hg19) ; chr22:g.19940984_19940985insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19940985dup , CM000684.2:g.19940985dup	GRCh38
NC_000022.10:g.19928508dup , CM000684.1:g.19928508dup	GRCh37
NC_000022.9:g.18308508dup	NCBI36
NG_011526.1:g.4246dup
NG_011835.1:g.5852dup , LRG_417:g.5852dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.103+716dup MANE Select	ENSP00000383365.1:n.103+716dup
ENST00000334363.14:c.103+716dup	ENSP00000334451.9:n.103+716dup
ENST00000400519.6:c.103+716dup	ENSP00000383363.1:n.103+716dup
ENST00000400521.6:c.103+716dup	ENSP00000383365.1:n.103+716dup
ENST00000400525.6:c.103+716dup	ENSP00000383369.3:n.103+716dup
ENST00000474308.5:c.103+716dup	ENSP00000485665.1:n.103+716dup
ENST00000496729.2:n.108+716dup
NM_001282512.1:c.103+716dup	NP_001269441.1:n.103+716dup
NM_006440.4:c.103+716dup	NP_006431.2:n.103+716dup
NM_001282512.2:c.103+716dup	NP_001269441.1:n.103+716dup
NM_001352300.1:c.103+716dup	NP_001339229.1:n.103+716dup
NR_147957.1:n.292+716dup
NM_006440.5:c.103+716dup MANE Select	NP_006431.2:n.103+716dup
NM_001282512.3:c.103+716dup	NP_001269441.1:n.103+716dup
NM_001352300.2:c.103+716dup	NP_001339229.1:n.103+716dup
NR_147957.2:n.118+716dup