Canonical Allele Identifier: CA410689667
Gene: COMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19964186G>C , CM000684.2:g.19964186G>C GRCh38
NC_000022.10:g.19951709G>C , CM000684.1:g.19951709G>C GRCh37
NC_000022.9:g.18331709G>C NCBI36
NG_011526.1:g.27447G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000361682.11:c.502G>C MANE Select ENSP00000354511.6:p.Ala168Pro
ENST00000428707.2:c.502G>C ENSP00000387695.2:p.Ala168Pro
ENST00000676678.1:c.502G>C ENSP00000503719.1:p.Ala168Pro
ENST00000677397.1:c.352G>C ENSP00000503422.1:p.Ala118Pro
ENST00000677470.1:n.352G>C
ENST00000677564.1:n.285G>C
ENST00000677675.1:n.302G>C
ENST00000678240.1:n.350G>C
ENST00000678255.1:c.502G>C ENSP00000504402.1:p.Ala168Pro
ENST00000678769.1:c.502G>C ENSP00000503289.1:p.Ala168Pro
ENST00000678868.1:c.502G>C ENSP00000503583.1:p.Ala168Pro
ENST00000678945.1:n.370G>C
ENST00000207636.9:c.560G>C ENSP00000207636.5:p.Ser187Thr
ENST00000361682.10:c.502G>C ENSP00000354511.6:p.Ala168Pro
ENST00000403184.5:c.502G>C ENSP00000383966.1:p.Ala168Pro
ENST00000403710.5:c.502G>C ENSP00000385917.1:p.Ala168Pro
ENST00000406520.7:c.502G>C ENSP00000385150.3:p.Ala168Pro
ENST00000407537.5:c.502G>C ENSP00000384654.2:p.Ala168Pro
ENST00000412786.5:c.502G>C ENSP00000403958.1:p.Ala168Pro
ENST00000428707.1:c.80G>C
ENST00000449653.5:c.352G>C ENSP00000416778.1:p.Ala118Pro
ENST00000493893.1:n.240G>C
NM_000754.3:c.502G>C NP_000745.1:p.Ala168Pro
NM_001135161.1:c.502G>C NP_001128633.1:p.Ala168Pro
NM_001135162.1:c.502G>C NP_001128634.1:p.Ala168Pro
NM_007310.2:c.352G>C NP_009294.1:p.Ala118Pro
XM_011529885.1:c.616G>C XP_011528187.1:p.Ala206Pro
XM_011529886.1:c.616G>C XP_011528188.1:p.Ala206Pro
XM_011529887.1:c.502G>C XP_011528189.1:p.Ala168Pro
XM_011529888.1:c.502G>C XP_011528190.1:p.Ala168Pro
XM_011529889.1:c.502G>C XP_011528191.1:p.Ala168Pro
XM_011529890.1:c.502G>C XP_011528192.1:p.Ala168Pro
XM_011529891.1:c.502G>C XP_011528193.1:p.Ala168Pro
NM_001362828.1:c.502G>C NP_001349757.1:p.Ala168Pro
XM_011529886.2:c.913G>C XP_011528188.2:p.Ala305Pro
XM_017028595.1:c.502G>C XP_016884084.1:p.Ala168Pro
NM_000754.4:c.502G>C MANE Select NP_000745.1:p.Ala168Pro
NM_001135161.2:c.502G>C NP_001128633.1:p.Ala168Pro
NM_001135162.2:c.502G>C NP_001128634.1:p.Ala168Pro
NM_001362828.2:c.502G>C NP_001349757.1:p.Ala168Pro
NM_007310.3:c.352G>C NP_009294.1:p.Ala118Pro