Canonical Allele Identifier: CA2396084850

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880667C= , CM000684.2:g.19880667C=	GRCh38
NC_000022.10:g.19868190C= , CM000684.1:g.19868190C=	GRCh37
NC_000022.9:g.18248190C=	NCBI36
NG_011835.1:g.66170G= , LRG_417:g.66170G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1137G= MANE Select	ENSP00000383365.1:p.Val379=
ENST00000400518.5:c.1047G=	ENSP00000383362.1:p.Val349=
ENST00000400519.6:c.1134G=	ENSP00000383363.1:p.Val378=
ENST00000400521.6:c.1137G=	ENSP00000383365.1:p.Val379=
ENST00000400525.6:c.1068G=	ENSP00000383369.3:p.Val356=
ENST00000462330.5:c.60G=	ENSP00000485603.2:p.Val20=
ENST00000462843.2:c.87G=	ENSP00000485466.2:p.Val29=
ENST00000474308.5:c.1080G=	ENSP00000485665.1:p.Val360=
ENST00000485358.5:c.105G=	ENSP00000485499.2:p.Val35=
ENST00000487165.5:n.1231G=
ENST00000494454.5:n.1211G=
ENST00000495655.2:n.681G=
ENST00000542719.6:c.849G=	ENSP00000485128.2:p.Val283=
ENST00000634471.1:n.244-396G=
ENST00000634537.1:c.366G=	ENSP00000489208.1:p.Val122=
NM_006440.4:c.1137G=	NP_006431.2:p.Val379=
NM_001352300.1:c.1134G=	NP_001339229.1:p.Val378=
NM_001352301.1:c.1047G=	NP_001339230.1:p.Val349=
NM_001352302.1:c.849G=	NP_001339231.1:p.Val283=
NR_147957.1:n.1269G=
NM_006440.5:c.1137G= MANE Select	NP_006431.2:p.Val379=
NM_001352300.2:c.1134G=	NP_001339229.1:p.Val378=
NR_147957.2:n.1095G=
NM_001352301.2:c.1047G=	NP_001339230.1:p.Val349=
NM_001352302.2:c.849G=	NP_001339231.1:p.Val283=