Canonical Allele Identifier: CA410686614

Gene: TXNRD2

Linked Data

• dbSNP Id: rs1939463686
• gnomAD v3: 22-19895491-C-T
• gnomAD v4: 22-19895491-C-T
• MyVariant Identifiers: chr22:g.19883014C>T (hg19) ; chr22:g.19895491C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895491C>T , CM000684.2:g.19895491C>T	GRCh38
NC_000022.10:g.19883014C>T , CM000684.1:g.19883014C>T	GRCh37
NC_000022.9:g.18263014C>T	NCBI36
NG_011835.1:g.51346G>A , LRG_417:g.51346G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.865G>A MANE Select	ENSP00000383365.1:p.Asp289Asn
ENST00000334363.14:c.865G>A	ENSP00000334451.9:p.Asp289Asn
ENST00000400518.5:c.775G>A	ENSP00000383362.1:p.Asp259Asn
ENST00000400519.6:c.862G>A	ENSP00000383363.1:p.Asp288Asn
ENST00000400521.6:c.865G>A	ENSP00000383365.1:p.Asp289Asn
ENST00000400525.6:c.796G>A	ENSP00000383369.3:p.Asp266Asn
ENST00000474308.5:c.808G>A	ENSP00000485665.1:p.Asp270Asn
ENST00000475995.3:c.362G>A
ENST00000491939.6:c.769G>A	ENSP00000485543.1:p.Asp257Asn
ENST00000494454.5:n.939G>A
ENST00000542719.6:c.577G>A	ENSP00000485128.2:p.Asp193Asn
ENST00000634537.1:c.94G>A	ENSP00000489208.1:p.Asp32Asn
ENST00000635155.1:n.451G>A
NM_001282512.1:c.865G>A	NP_001269441.1:p.Asp289Asn
NM_006440.4:c.865G>A	NP_006431.2:p.Asp289Asn
NM_001282512.2:c.865G>A	NP_001269441.1:p.Asp289Asn
NM_001352300.1:c.862G>A	NP_001339229.1:p.Asp288Asn
NM_001352301.1:c.775G>A	NP_001339230.1:p.Asp259Asn
NM_001352302.1:c.577G>A	NP_001339231.1:p.Asp193Asn
NM_001352303.1:c.769G>A	NP_001339232.1:p.Asp257Asn
NR_147957.1:n.997G>A
NM_006440.5:c.865G>A MANE Select	NP_006431.2:p.Asp289Asn
NM_001282512.3:c.865G>A	NP_001269441.1:p.Asp289Asn
NM_001352300.2:c.862G>A	NP_001339229.1:p.Asp288Asn
NR_147957.2:n.823G>A
NM_001352301.2:c.775G>A	NP_001339230.1:p.Asp259Asn
NM_001352302.2:c.577G>A	NP_001339231.1:p.Asp193Asn
NM_001352303.2:c.769G>A	NP_001339232.1:p.Asp257Asn