Canonical Allele Identifier: CA10103810

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880738del , CM000684.2:g.19880738del	GRCh38
NC_000022.10:g.19868261del , CM000684.1:g.19868261del	GRCh37
NC_000022.9:g.18248261del	NCBI36
NG_011835.1:g.66104del , LRG_417:g.66104del

Transcript Alleles

HGVS	Amino-acid Change
NM_006440.5:c.1087-16del MANE Select	NP_006431.2:n.1087-16del
ENST00000400521.7:c.1087-16del MANE Select	ENSP00000383365.1:n.1087-16del
NM_001352300.1:c.1084-16del	NP_001339229.1:n.1084-16del
NM_001352300.2:c.1084-16del	NP_001339229.1:n.1084-16del
NM_001352301.1:c.997-16del	NP_001339230.1:n.997-16del
NM_001352301.2:c.997-16del	NP_001339230.1:n.997-16del
NM_001352302.1:c.799-16del	NP_001339231.1:n.799-16del
NM_001352302.2:c.799-16del	NP_001339231.1:n.799-16del
NM_006440.4:c.1087-16del	NP_006431.2:n.1087-16del
NR_147957.1:n.1219-16del
NR_147957.2:n.1045-16del
ENST00000400518.5:c.997-16del	ENSP00000383362.1:n.997-16del
ENST00000400519.6:c.1084-16del	ENSP00000383363.1:n.1084-16del
ENST00000400521.6:c.1087-16del	ENSP00000383365.1:n.1087-16del
ENST00000400525.6:c.1018-16del	ENSP00000383369.3:n.1018-16del
ENST00000462330.5:c.10-16del	ENSP00000485603.2:n.10-16del
ENST00000462843.2:c.37-16del	ENSP00000485466.2:n.37-16del
ENST00000474308.5:c.1030-16del	ENSP00000485665.1:n.1030-16del
ENST00000485358.5:c.55-16del	ENSP00000485499.2:n.55-16del
ENST00000487165.5:n.1181-16del
ENST00000494454.5:n.1161-16del
ENST00000495655.2:n.615del
ENST00000542719.6:c.799-16del	ENSP00000485128.2:n.799-16del
ENST00000634471.1:n.244-462del
ENST00000634537.1:c.316-16del	ENSP00000489208.1:n.316-16del