Canonical Allele Identifier: CA410681903

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19868156C>G (hg19) ; chr22:g.19880633C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880633C>G , CM000684.2:g.19880633C>G	GRCh38
NC_000022.10:g.19868156C>G , CM000684.1:g.19868156C>G	GRCh37
NC_000022.9:g.18248156C>G	NCBI36
NG_011835.1:g.66204G>C , LRG_417:g.66204G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.1171G>C MANE Select	ENSP00000383365.1:p.Asp391His
ENST00000400518.5:c.1081G>C	ENSP00000383362.1:p.Asp361His
ENST00000400519.6:c.1168G>C	ENSP00000383363.1:p.Asp390His
ENST00000400521.6:c.1171G>C	ENSP00000383365.1:p.Asp391His
ENST00000400525.6:c.1102G>C	ENSP00000383369.3:p.Asp368His
ENST00000462330.5:c.94G>C	ENSP00000485603.2:p.Asp32His
ENST00000462843.2:c.121G>C	ENSP00000485466.2:p.Asp41His
ENST00000474308.5:c.1114G>C	ENSP00000485665.1:p.Asp372His
ENST00000485358.5:c.139G>C	ENSP00000485499.2:p.Asp47His
ENST00000487165.5:n.1265G>C
ENST00000494454.5:n.1245G>C
ENST00000495655.2:n.715G>C
ENST00000542719.6:c.883G>C	ENSP00000485128.2:p.Asp295His
ENST00000634471.1:n.244-362G>C
ENST00000634537.1:c.400G>C	ENSP00000489208.1:p.Asp134His
NM_006440.4:c.1171G>C	NP_006431.2:p.Asp391His
NM_001352300.1:c.1168G>C	NP_001339229.1:p.Asp390His
NM_001352301.1:c.1081G>C	NP_001339230.1:p.Asp361His
NM_001352302.1:c.883G>C	NP_001339231.1:p.Asp295His
NR_147957.1:n.1303G>C
NM_006440.5:c.1171G>C MANE Select	NP_006431.2:p.Asp391His
NM_001352300.2:c.1168G>C	NP_001339229.1:p.Asp390His
NR_147957.2:n.1129G>C
NM_001352301.2:c.1081G>C	NP_001339230.1:p.Asp361His
NM_001352302.2:c.883G>C	NP_001339231.1:p.Asp295His