Canonical Allele Identifier: CA513361620

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19880640-A-G
• MyVariant Identifiers: chr22:g.19868163A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880640A>G , CM000684.2:g.19880640A>G	GRCh38
NC_000022.10:g.19868163A>G , CM000684.1:g.19868163A>G	GRCh37
NC_000022.9:g.18248163A>G	NCBI36
NG_011835.1:g.66197T>C , LRG_417:g.66197T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.1164T>C MANE Select	ENSP00000383365.1:p.Asp388=
ENST00000400518.5:c.1074T>C	ENSP00000383362.1:p.Asp358=
ENST00000400519.6:c.1161T>C	ENSP00000383363.1:p.Asp387=
ENST00000400521.6:c.1164T>C	ENSP00000383365.1:p.Asp388=
ENST00000400525.6:c.1095T>C	ENSP00000383369.3:p.Asp365=
ENST00000462330.5:c.87T>C	ENSP00000485603.2:p.Asp29=
ENST00000462843.2:c.114T>C	ENSP00000485466.2:p.Asp38=
ENST00000474308.5:c.1107T>C	ENSP00000485665.1:p.Asp369=
ENST00000485358.5:c.132T>C	ENSP00000485499.2:p.Asp44=
ENST00000487165.5:n.1258T>C
ENST00000494454.5:n.1238T>C
ENST00000495655.2:n.708T>C
ENST00000542719.6:c.876T>C	ENSP00000485128.2:p.Asp292=
ENST00000634471.1:n.244-369T>C
ENST00000634537.1:c.393T>C	ENSP00000489208.1:p.Asp131=
NM_006440.4:c.1164T>C	NP_006431.2:p.Asp388=
NM_001352300.1:c.1161T>C	NP_001339229.1:p.Asp387=
NM_001352301.1:c.1074T>C	NP_001339230.1:p.Asp358=
NM_001352302.1:c.876T>C	NP_001339231.1:p.Asp292=
NR_147957.1:n.1296T>C
NM_006440.5:c.1164T>C MANE Select	NP_006431.2:p.Asp388=
NM_001352300.2:c.1161T>C	NP_001339229.1:p.Asp387=
NR_147957.2:n.1122T>C
NM_001352301.2:c.1074T>C	NP_001339230.1:p.Asp358=
NM_001352302.2:c.876T>C	NP_001339231.1:p.Asp292=