Canonical Allele Identifier: CA410681901

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19868155T>A (hg19) ; chr22:g.19880632T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880632T>A , CM000684.2:g.19880632T>A	GRCh38
NC_000022.10:g.19868155T>A , CM000684.1:g.19868155T>A	GRCh37
NC_000022.9:g.18248155T>A	NCBI36
NG_011835.1:g.66205A>T , LRG_417:g.66205A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.1172A>T MANE Select	ENSP00000383365.1:p.Asp391Val
ENST00000400518.5:c.1082A>T	ENSP00000383362.1:p.Asp361Val
ENST00000400519.6:c.1169A>T	ENSP00000383363.1:p.Asp390Val
ENST00000400521.6:c.1172A>T	ENSP00000383365.1:p.Asp391Val
ENST00000400525.6:c.1103A>T	ENSP00000383369.3:p.Asp368Val
ENST00000462330.5:c.95A>T	ENSP00000485603.2:p.Asp32Val
ENST00000462843.2:c.122A>T	ENSP00000485466.2:p.Asp41Val
ENST00000474308.5:c.1115A>T	ENSP00000485665.1:p.Asp372Val
ENST00000485358.5:c.140A>T	ENSP00000485499.2:p.Asp47Val
ENST00000487165.5:n.1266A>T
ENST00000494454.5:n.1246A>T
ENST00000495655.2:n.716A>T
ENST00000542719.6:c.884A>T	ENSP00000485128.2:p.Asp295Val
ENST00000634471.1:n.244-361A>T
ENST00000634537.1:c.401A>T	ENSP00000489208.1:p.Asp134Val
NM_006440.4:c.1172A>T	NP_006431.2:p.Asp391Val
NM_001352300.1:c.1169A>T	NP_001339229.1:p.Asp390Val
NM_001352301.1:c.1082A>T	NP_001339230.1:p.Asp361Val
NM_001352302.1:c.884A>T	NP_001339231.1:p.Asp295Val
NR_147957.1:n.1304A>T
NM_006440.5:c.1172A>T MANE Select	NP_006431.2:p.Asp391Val
NM_001352300.2:c.1169A>T	NP_001339229.1:p.Asp390Val
NR_147957.2:n.1130A>T
NM_001352301.2:c.1082A>T	NP_001339230.1:p.Asp361Val
NM_001352302.2:c.884A>T	NP_001339231.1:p.Asp295Val