Canonical Allele Identifier: CA410682657

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19883353T>G , CM000684.2:g.19883353T>G	GRCh38
NC_000022.10:g.19870876T>G , CM000684.1:g.19870876T>G	GRCh37
NC_000022.9:g.18250876T>G	NCBI36
NG_011835.1:g.63484A>C , LRG_417:g.63484A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006440.5:c.1058A>C MANE Select	NP_006431.2:p.His353Pro
ENST00000400521.7:c.1058A>C MANE Select	ENSP00000383365.1:p.His353Pro
NM_001352300.1:c.1055A>C	NP_001339229.1:p.His352Pro
NM_001352300.2:c.1055A>C	NP_001339229.1:p.His352Pro
NM_001352301.1:c.968A>C	NP_001339230.1:p.His323Pro
NM_001352301.2:c.968A>C	NP_001339230.1:p.His323Pro
NM_001352302.1:c.770A>C	NP_001339231.1:p.His257Pro
NM_001352302.2:c.770A>C	NP_001339231.1:p.His257Pro
NM_006440.4:c.1058A>C	NP_006431.2:p.His353Pro
NR_147957.1:n.1190A>C
NR_147957.2:n.1016A>C
ENST00000400518.5:c.968A>C	ENSP00000383362.1:p.His323Pro
ENST00000400519.6:c.1055A>C	ENSP00000383363.1:p.His352Pro
ENST00000400521.6:c.1058A>C	ENSP00000383365.1:p.His353Pro
ENST00000400525.6:c.989A>C	ENSP00000383369.3:p.His330Pro
ENST00000474308.5:c.1001A>C	ENSP00000485665.1:p.His334Pro
ENST00000487165.5:n.1152A>C
ENST00000494454.5:n.1132A>C
ENST00000542719.6:c.770A>C	ENSP00000485128.2:p.His257Pro
ENST00000634471.1:n.215A>C
ENST00000634537.1:c.287A>C	ENSP00000489208.1:p.His96Pro