Canonical Allele Identifier: CA10104651
Gene: COMT HGNC NCBI

Linked Data

dbSNP Id: rs377403244

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19964286C>T , CM000684.2:g.19964286C>T GRCh38
NC_000022.10:g.19951809C>T , CM000684.1:g.19951809C>T GRCh37
NC_000022.9:g.18331809C>T NCBI36
NG_011526.1:g.27547C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000361682.11:c.602C>T MANE Select ENSP00000354511.6:p.Thr201Met
ENST00000428707.2:c.602C>T ENSP00000387695.2:p.Thr201Met
ENST00000676678.1:c.602C>T ENSP00000503719.1:p.Thr201Met
ENST00000677397.1:c.452C>T ENSP00000503422.1:p.Thr151Met
ENST00000677470.1:n.452C>T
ENST00000677564.1:n.385C>T
ENST00000677675.1:n.402C>T
ENST00000678240.1:n.450C>T
ENST00000678255.1:c.602C>T ENSP00000504402.1:p.Thr201Met
ENST00000678769.1:c.602C>T ENSP00000503289.1:p.Thr201Met
ENST00000678868.1:c.602C>T ENSP00000503583.1:p.Thr201Met
ENST00000678945.1:n.470C>T
ENST00000207636.9:c.*60C>T ENSP00000207636.5:n.*60C>T
ENST00000361682.10:c.602C>T ENSP00000354511.6:p.Thr201Met
ENST00000403184.5:c.602C>T ENSP00000383966.1:p.Thr201Met
ENST00000403710.5:c.602C>T ENSP00000385917.1:p.Thr201Met
ENST00000406520.7:c.602C>T ENSP00000385150.3:p.Thr201Met
ENST00000407537.5:c.602C>T ENSP00000384654.2:p.Thr201Met
ENST00000412786.5:c.602C>T ENSP00000403958.1:p.Thr201Met
ENST00000428707.1:c.180C>T
ENST00000449653.5:c.452C>T ENSP00000416778.1:p.Thr151Met
ENST00000493893.1:n.340C>T
NM_000754.3:c.602C>T NP_000745.1:p.Thr201Met
NM_001135161.1:c.602C>T NP_001128633.1:p.Thr201Met
NM_001135162.1:c.602C>T NP_001128634.1:p.Thr201Met
NM_007310.2:c.452C>T NP_009294.1:p.Thr151Met
XM_011529885.1:c.716C>T XP_011528187.1:p.Thr239Met
XM_011529886.1:c.716C>T XP_011528188.1:p.Thr239Met
XM_011529887.1:c.602C>T XP_011528189.1:p.Thr201Met
XM_011529888.1:c.602C>T XP_011528190.1:p.Thr201Met
XM_011529889.1:c.602C>T XP_011528191.1:p.Thr201Met
XM_011529890.1:c.602C>T XP_011528192.1:p.Thr201Met
XM_011529891.1:c.602C>T XP_011528193.1:p.Thr201Met
NM_001362828.1:c.602C>T NP_001349757.1:p.Thr201Met
XM_011529886.2:c.1013C>T XP_011528188.2:p.Thr338Met
XM_017028595.1:c.602C>T XP_016884084.1:p.Thr201Met
NM_000754.4:c.602C>T MANE Select NP_000745.1:p.Thr201Met
NM_001135161.2:c.602C>T NP_001128633.1:p.Thr201Met
NM_001135162.2:c.602C>T NP_001128634.1:p.Thr201Met
NM_001362828.2:c.602C>T NP_001349757.1:p.Thr201Met
NM_007310.3:c.452C>T NP_009294.1:p.Thr151Met