Canonical Allele Identifier: CA2396084893

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880729C= , CM000684.2:g.19880729C=	GRCh38
NC_000022.10:g.19868252C= , CM000684.1:g.19868252C=	GRCh37
NC_000022.9:g.18248252C=	NCBI36
NG_011835.1:g.66108G= , LRG_417:g.66108G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1087-12G= MANE Select	ENSP00000383365.1:n.1087-12G=
ENST00000400518.5:c.997-12G=	ENSP00000383362.1:n.997-12G=
ENST00000400519.6:c.1084-12G=	ENSP00000383363.1:n.1084-12G=
ENST00000400521.6:c.1087-12G=	ENSP00000383365.1:n.1087-12G=
ENST00000400525.6:c.1018-12G=	ENSP00000383369.3:n.1018-12G=
ENST00000462330.5:c.10-12G=	ENSP00000485603.2:n.10-12G=
ENST00000462843.2:c.37-12G=	ENSP00000485466.2:n.37-12G=
ENST00000474308.5:c.1030-12G=	ENSP00000485665.1:n.1030-12G=
ENST00000485358.5:c.55-12G=	ENSP00000485499.2:n.55-12G=
ENST00000487165.5:n.1181-12G=
ENST00000494454.5:n.1161-12G=
ENST00000495655.2:n.619G=
ENST00000542719.6:c.799-12G=	ENSP00000485128.2:n.799-12G=
ENST00000634471.1:n.244-458G=
ENST00000634537.1:c.316-12G=	ENSP00000489208.1:n.316-12G=
NM_006440.4:c.1087-12G=	NP_006431.2:n.1087-12G=
NM_001352300.1:c.1084-12G=	NP_001339229.1:n.1084-12G=
NM_001352301.1:c.997-12G=	NP_001339230.1:n.997-12G=
NM_001352302.1:c.799-12G=	NP_001339231.1:n.799-12G=
NR_147957.1:n.1219-12G=
NM_006440.5:c.1087-12G= MANE Select	NP_006431.2:n.1087-12G=
NM_001352300.2:c.1084-12G=	NP_001339229.1:n.1084-12G=
NR_147957.2:n.1045-12G=
NM_001352301.2:c.997-12G=	NP_001339230.1:n.997-12G=
NM_001352302.2:c.799-12G=	NP_001339231.1:n.799-12G=