Canonical Allele Identifier: CA410686375

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19882953A>G (hg19) ; chr22:g.19895430A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895430A>G , CM000684.2:g.19895430A>G	GRCh38
NC_000022.10:g.19882953A>G , CM000684.1:g.19882953A>G	GRCh37
NC_000022.9:g.18262953A>G	NCBI36
NG_011835.1:g.51407T>C , LRG_417:g.51407T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.926T>C MANE Select	ENSP00000383365.1:p.Phe309Ser
ENST00000334363.14:c.926T>C	ENSP00000334451.9:p.Phe309Ser
ENST00000400518.5:c.836T>C	ENSP00000383362.1:p.Phe279Ser
ENST00000400519.6:c.923T>C	ENSP00000383363.1:p.Phe308Ser
ENST00000400521.6:c.926T>C	ENSP00000383365.1:p.Phe309Ser
ENST00000400525.6:c.857T>C	ENSP00000383369.3:p.Phe286Ser
ENST00000474308.5:c.869T>C	ENSP00000485665.1:p.Phe290Ser
ENST00000475995.3:c.423T>C
ENST00000491939.6:c.830T>C	ENSP00000485543.1:p.Phe277Ser
ENST00000494454.5:n.1000T>C
ENST00000542719.6:c.638T>C	ENSP00000485128.2:p.Phe213Ser
ENST00000634537.1:c.155T>C	ENSP00000489208.1:p.Phe52Ser
ENST00000635155.1:n.512T>C
NM_001282512.1:c.926T>C	NP_001269441.1:p.Phe309Ser
NM_006440.4:c.926T>C	NP_006431.2:p.Phe309Ser
NM_001282512.2:c.926T>C	NP_001269441.1:p.Phe309Ser
NM_001352300.1:c.923T>C	NP_001339229.1:p.Phe308Ser
NM_001352301.1:c.836T>C	NP_001339230.1:p.Phe279Ser
NM_001352302.1:c.638T>C	NP_001339231.1:p.Phe213Ser
NM_001352303.1:c.830T>C	NP_001339232.1:p.Phe277Ser
NR_147957.1:n.1058T>C
NM_006440.5:c.926T>C MANE Select	NP_006431.2:p.Phe309Ser
NM_001282512.3:c.926T>C	NP_001269441.1:p.Phe309Ser
NM_001352300.2:c.923T>C	NP_001339229.1:p.Phe308Ser
NR_147957.2:n.884T>C
NM_001352301.2:c.836T>C	NP_001339230.1:p.Phe279Ser
NM_001352302.2:c.638T>C	NP_001339231.1:p.Phe213Ser
NM_001352303.2:c.830T>C	NP_001339232.1:p.Phe277Ser