Canonical Allele Identifier: CA2396084831

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880635A= , CM000684.2:g.19880635A=	GRCh38
NC_000022.10:g.19868158A= , CM000684.1:g.19868158A=	GRCh37
NC_000022.9:g.18248158A=	NCBI36
NG_011835.1:g.66202T= , LRG_417:g.66202T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.1169T= MANE Select	ENSP00000383365.1:p.Met390=
ENST00000400518.5:c.1079T=	ENSP00000383362.1:p.Met360=
ENST00000400519.6:c.1166T=	ENSP00000383363.1:p.Met389=
ENST00000400521.6:c.1169T=	ENSP00000383365.1:p.Met390=
ENST00000400525.6:c.1100T=	ENSP00000383369.3:p.Met367=
ENST00000462330.5:c.92T=	ENSP00000485603.2:p.Met31=
ENST00000462843.2:c.119T=	ENSP00000485466.2:p.Met40=
ENST00000474308.5:c.1112T=	ENSP00000485665.1:p.Met371=
ENST00000485358.5:c.137T=	ENSP00000485499.2:p.Met46=
ENST00000487165.5:n.1263T=
ENST00000494454.5:n.1243T=
ENST00000495655.2:n.713T=
ENST00000542719.6:c.881T=	ENSP00000485128.2:p.Met294=
ENST00000634471.1:n.244-364T=
ENST00000634537.1:c.398T=	ENSP00000489208.1:p.Met133=
NM_006440.4:c.1169T=	NP_006431.2:p.Met390=
NM_001352300.1:c.1166T=	NP_001339229.1:p.Met389=
NM_001352301.1:c.1079T=	NP_001339230.1:p.Met360=
NM_001352302.1:c.881T=	NP_001339231.1:p.Met294=
NR_147957.1:n.1301T=
NM_006440.5:c.1169T= MANE Select	NP_006431.2:p.Met390=
NM_001352300.2:c.1166T=	NP_001339229.1:p.Met389=
NR_147957.2:n.1127T=
NM_001352301.2:c.1079T=	NP_001339230.1:p.Met360=
NM_001352302.2:c.881T=	NP_001339231.1:p.Met294=