Canonical Allele Identifier: CA16616529

Gene: TXNRD2 COMT

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19941727A>C , CM000684.2:g.19941727A>C	GRCh38
NC_000022.10:g.19929250A>C , CM000684.1:g.19929250A>C	GRCh37
NC_000022.9:g.18309250A>C	NCBI36
NG_011526.1:g.4988A>C
NG_011835.1:g.5110T>G , LRG_417:g.5110T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006440.5:c.77T>G (TXNRD2) MANE Select	NP_006431.2:p.Val26Gly
ENST00000400521.7:c.77T>G (TXNRD2) MANE Select	ENSP00000383365.1:p.Val26Gly
NM_001282512.1:c.77T>G (TXNRD2)	NP_001269441.1:p.Val26Gly
NM_001282512.2:c.77T>G (TXNRD2)	NP_001269441.1:p.Val26Gly
NM_001282512.3:c.77T>G (TXNRD2)	NP_001269441.1:p.Val26Gly
NM_001352300.1:c.77T>G (TXNRD2)	NP_001339229.1:p.Val26Gly
NM_001352300.2:c.77T>G (TXNRD2)	NP_001339229.1:p.Val26Gly
NM_006440.4:c.77T>G (TXNRD2)	NP_006431.2:p.Val26Gly
NR_147957.1:n.266T>G (TXNRD2)
NR_147957.2:n.92T>G (TXNRD2)
ENST00000334363.14:c.77T>G (TXNRD2)	ENSP00000334451.9:p.Val26Gly
ENST00000361682.10:c.-262A>C (COMT)	ENSP00000354511.6:n.-262A>C
ENST00000400519.6:c.77T>G (TXNRD2)	ENSP00000383363.1:p.Val26Gly
ENST00000400521.6:c.77T>G (TXNRD2)	ENSP00000383365.1:p.Val26Gly
ENST00000400525.6:c.77T>G (TXNRD2)	ENSP00000383369.3:p.Val26Gly
ENST00000474308.5:c.77T>G (TXNRD2)	ENSP00000485665.1:p.Val26Gly
ENST00000496729.2:n.82T>G (TXNRD2)
ENST00000676678.1:c.-92+152A>C (COMT)	ENSP00000503719.1:n.-92+152A>C