Canonical Allele Identifier: CA2396084829

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880631G= , CM000684.2:g.19880631G=	GRCh38
NC_000022.10:g.19868154G= , CM000684.1:g.19868154G=	GRCh37
NC_000022.9:g.18248154G=	NCBI36
NG_011835.1:g.66206C= , LRG_417:g.66206C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.1173C= MANE Select	ENSP00000383365.1:p.Asp391=
ENST00000400518.5:c.1083C=	ENSP00000383362.1:p.Asp361=
ENST00000400519.6:c.1170C=	ENSP00000383363.1:p.Asp390=
ENST00000400521.6:c.1173C=	ENSP00000383365.1:p.Asp391=
ENST00000400525.6:c.1104C=	ENSP00000383369.3:p.Asp368=
ENST00000462330.5:c.96C=	ENSP00000485603.2:p.Asp32=
ENST00000462843.2:c.123C=	ENSP00000485466.2:p.Asp41=
ENST00000474308.5:c.1116C=	ENSP00000485665.1:p.Asp372=
ENST00000485358.5:c.141C=	ENSP00000485499.2:p.Asp47=
ENST00000487165.5:n.1267C=
ENST00000494454.5:n.1247C=
ENST00000495655.2:n.717C=
ENST00000542719.6:c.885C=	ENSP00000485128.2:p.Asp295=
ENST00000634471.1:n.244-360C=
ENST00000634537.1:c.402C=	ENSP00000489208.1:p.Asp134=
NM_006440.4:c.1173C=	NP_006431.2:p.Asp391=
NM_001352300.1:c.1170C=	NP_001339229.1:p.Asp390=
NM_001352301.1:c.1083C=	NP_001339230.1:p.Asp361=
NM_001352302.1:c.885C=	NP_001339231.1:p.Asp295=
NR_147957.1:n.1305C=
NM_006440.5:c.1173C= MANE Select	NP_006431.2:p.Asp391=
NM_001352300.2:c.1170C=	NP_001339229.1:p.Asp390=
NR_147957.2:n.1131C=
NM_001352301.2:c.1083C=	NP_001339230.1:p.Asp361=
NM_001352302.2:c.885C=	NP_001339231.1:p.Asp295=