Canonical Allele Identifier: CA2396103696
Gene: TXNRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19918819T= , CM000684.2:g.19918819T= GRCh38
NC_000022.10:g.19906342T= , CM000684.1:g.19906342T= GRCh37
NC_000022.9:g.18286342T= NCBI36
NG_011835.1:g.28018A= , LRG_417:g.28018A=

Transcript Alleles

HGVS Amino-acid change
ENST00000400521.7:c.374+41A= MANE Select ENSP00000383365.1:n.374+41A=
ENST00000334363.14:c.374+41A= ENSP00000334451.9:n.374+41A=
ENST00000400518.5:c.284+41A= ENSP00000383362.1:n.284+41A=
ENST00000400519.6:c.371+41A= ENSP00000383363.1:n.371+41A=
ENST00000400521.6:c.374+41A= ENSP00000383365.1:n.374+41A=
ENST00000400525.6:c.305+41A= ENSP00000383369.3:n.305+41A=
ENST00000474308.5:c.317+41A= ENSP00000485665.1:n.317+41A=
ENST00000491939.6:c.278+41A= ENSP00000485543.1:n.278+41A=
ENST00000496729.2:n.379+41A=
ENST00000542719.6:c.86+41A= ENSP00000485128.2:n.86+41A=
NM_001282512.1:c.374+41A= NP_001269441.1:n.374+41A=
NM_006440.4:c.374+41A= NP_006431.2:n.374+41A=
NM_001282512.2:c.374+41A= NP_001269441.1:n.374+41A=
NM_001352300.1:c.371+41A= NP_001339229.1:n.371+41A=
NM_001352301.1:c.284+41A= NP_001339230.1:n.284+41A=
NM_001352302.1:c.86+41A= NP_001339231.1:n.86+41A=
NM_001352303.1:c.278+41A= NP_001339232.1:n.278+41A=
NR_147957.1:n.506+41A=
NM_006440.5:c.374+41A= MANE Select NP_006431.2:n.374+41A=
NM_001282512.3:c.374+41A= NP_001269441.1:n.374+41A=
NM_001352300.2:c.371+41A= NP_001339229.1:n.371+41A=
NR_147957.2:n.332+41A=
NM_001352301.2:c.284+41A= NP_001339230.1:n.284+41A=
NM_001352302.2:c.86+41A= NP_001339231.1:n.86+41A=
NM_001352303.2:c.278+41A= NP_001339232.1:n.278+41A=