Canonical Allele Identifier: CA2655323351

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19880547-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880547C>A , CM000684.2:g.19880547C>A	GRCh38
NC_000022.10:g.19868070C>A , CM000684.1:g.19868070C>A	GRCh37
NC_000022.9:g.18248070C>A	NCBI36
NG_011835.1:g.66290G>T , LRG_417:g.66290G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.1182+75G>T MANE Select	ENSP00000383365.1:n.1182+75G>T
ENST00000400518.5:c.1092+75G>T	ENSP00000383362.1:n.1092+75G>T
ENST00000400519.6:c.1179+75G>T	ENSP00000383363.1:n.1179+75G>T
ENST00000400521.6:c.1182+75G>T	ENSP00000383365.1:n.1182+75G>T
ENST00000400525.6:c.1113+75G>T	ENSP00000383369.3:n.1113+75G>T
ENST00000462330.5:c.105+75G>T	ENSP00000485603.2:n.105+75G>T
ENST00000462843.2:c.132+75G>T	ENSP00000485466.2:n.132+75G>T
ENST00000474308.5:c.1125+75G>T	ENSP00000485665.1:n.1125+75G>T
ENST00000485358.5:c.150+75G>T	ENSP00000485499.2:n.150+75G>T
ENST00000487165.5:n.1276+75G>T
ENST00000494454.5:n.1256+75G>T
ENST00000495655.2:n.726+75G>T
ENST00000542719.6:c.894+75G>T	ENSP00000485128.2:n.894+75G>T
ENST00000634471.1:n.244-276G>T
ENST00000634537.1:c.411+75G>T	ENSP00000489208.1:n.411+75G>T
NM_006440.4:c.1182+75G>T	NP_006431.2:n.1182+75G>T
NM_001352300.1:c.1179+75G>T	NP_001339229.1:n.1179+75G>T
NM_001352301.1:c.1092+75G>T	NP_001339230.1:n.1092+75G>T
NM_001352302.1:c.894+75G>T	NP_001339231.1:n.894+75G>T
NR_147957.1:n.1314+75G>T
NM_006440.5:c.1182+75G>T MANE Select	NP_006431.2:n.1182+75G>T
NM_001352300.2:c.1179+75G>T	NP_001339229.1:n.1179+75G>T
NR_147957.2:n.1140+75G>T
NM_001352301.2:c.1092+75G>T	NP_001339230.1:n.1092+75G>T
NM_001352302.2:c.894+75G>T	NP_001339231.1:n.894+75G>T