Canonical Allele Identifier: CA2060132502

Gene: TXNRD1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.104333966G= , CM000674.2:g.104333966G=	GRCh38
NC_000012.11:g.104727744G= , CM000674.1:g.104727744G=	GRCh37
NC_000012.10:g.103251874G=	NCBI36
NG_029392.1:g.123186G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001093771.3:c.1651-271G= MANE Select	NP_001087240.1:n.1651-271G=
ENST00000525566.6:c.1651-271G= MANE Select	ENSP00000434516.1:n.1651-271G=
NM_001093771.2:c.1651-271G=	NP_001087240.1:n.1651-271G=
NM_001261445.1:c.1351-271G=	NP_001248374.1:n.1351-271G=
NM_001261445.2:c.1351-271G=	NP_001248374.1:n.1351-271G=
NM_001261446.1:c.1087-271G=	NP_001248375.1:n.1087-271G=
NM_001261446.2:c.1087-271G=	NP_001248375.1:n.1087-271G=
NM_003330.3:c.1357-271G=	NP_003321.3:n.1357-271G=
NM_003330.4:c.1357-271G=	NP_003321.3:n.1357-271G=
NM_182729.2:c.1201-271G=	NP_877393.1:n.1201-271G=
NM_182729.3:c.1201-271G=	NP_877393.1:n.1201-271G=
NM_182742.2:c.1201-271G=	NP_877419.1:n.1201-271G=
NM_182742.3:c.1201-271G=	NP_877419.1:n.1201-271G=
NM_182743.2:c.1201-271G=	NP_877420.1:n.1201-271G=
NM_182743.3:c.1201-271G=	NP_877420.1:n.1201-271G=
ENST00000354940.10:c.1201-271G=	ENSP00000347020.7:n.1201-271G=
ENST00000388854.7:c.1351-271G=	ENSP00000373506.4:n.1351-271G=
ENST00000397736.6:c.1087-271G=	ENSP00000380844.3:n.1087-271G=
ENST00000429002.6:c.1651-271G=	ENSP00000412045.4:n.1651-271G=
ENST00000503506.6:c.1201-271G=	ENSP00000421934.2:n.1201-271G=
ENST00000524698.5:c.1201-271G=	ENSP00000433425.1:n.1201-271G=
ENST00000525566.5:c.1651-271G=	ENSP00000434516.1:n.1651-271G=
ENST00000526390.5:c.1333-271G=	ENSP00000435123.1:n.1333-271G=
ENST00000526691.5:c.1357-271G=	ENSP00000435929.1:n.1357-271G=
ENST00000526950.1:c.1408-271G=	ENSP00000432812.1:n.1408-271G=
ENST00000526950.2:c.1546-271G=	ENSP00000432812.2:n.1546-271G=
ENST00000527688.5:c.1201-271G=	ENSP00000433935.1:n.1201-271G=
ENST00000529546.5:c.1087-271G=	ENSP00000434919.1:n.1087-271G=