Canonical Allele Identifier: CA2655330856

Gene: TXNRD2 COMT

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19941504C>G , CM000684.2:g.19941504C>G	GRCh38
NC_000022.10:g.19929027C>G , CM000684.1:g.19929027C>G	GRCh37
NC_000022.9:g.18309027C>G	NCBI36
NG_011526.1:g.4765C>G
NG_011835.1:g.5333G>C , LRG_417:g.5333G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006440.5:c.103+197G>C (TXNRD2) MANE Select	NP_006431.2:n.103+197G>C
ENST00000400521.7:c.103+197G>C (TXNRD2) MANE Select	ENSP00000383365.1:n.103+197G>C
NM_001282512.1:c.103+197G>C (TXNRD2)	NP_001269441.1:n.103+197G>C
NM_001282512.2:c.103+197G>C (TXNRD2)	NP_001269441.1:n.103+197G>C
NM_001282512.3:c.103+197G>C (TXNRD2)	NP_001269441.1:n.103+197G>C
NM_001352300.1:c.103+197G>C (TXNRD2)	NP_001339229.1:n.103+197G>C
NM_001352300.2:c.103+197G>C (TXNRD2)	NP_001339229.1:n.103+197G>C
NM_006440.4:c.103+197G>C (TXNRD2)	NP_006431.2:n.103+197G>C
NR_147957.1:n.292+197G>C (TXNRD2)
NR_147957.2:n.118+197G>C (TXNRD2)
ENST00000334363.14:c.103+197G>C (TXNRD2)	ENSP00000334451.9:n.103+197G>C
ENST00000400519.6:c.103+197G>C (TXNRD2)	ENSP00000383363.1:n.103+197G>C
ENST00000400521.6:c.103+197G>C (TXNRD2)	ENSP00000383365.1:n.103+197G>C
ENST00000400525.6:c.103+197G>C (TXNRD2)	ENSP00000383369.3:n.103+197G>C
ENST00000474308.5:c.103+197G>C (TXNRD2)	ENSP00000485665.1:n.103+197G>C
ENST00000496729.2:n.108+197G>C (TXNRD2)
ENST00000676678.1:c.-163C>G (COMT)	ENSP00000503719.1:n.-163C>G