Canonical Allele Identifier: CA2396121011
Gene: COMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19953984A= , CM000684.2:g.19953984A= GRCh38
NC_000022.10:g.19941507A= , CM000684.1:g.19941507A= GRCh37
NC_000022.9:g.18321507A= NCBI36
NG_011526.1:g.17245A=

Transcript Alleles

HGVS Amino-acid Change
NM_000754.4:c.-91-7215A= MANE Select NP_000745.1:n.-91-7215A=
ENST00000361682.11:c.-91-7215A= MANE Select ENSP00000354511.6:n.-91-7215A=
NM_000754.3:c.-91-7215A= NP_000745.1:n.-91-7215A=
NM_001135161.1:c.-92+2932A= NP_001128633.1:n.-92+2932A=
NM_001135161.2:c.-92+2932A= NP_001128633.1:n.-92+2932A=
NM_001135162.1:c.-92+2330A= NP_001128634.1:n.-92+2330A=
NM_001135162.2:c.-92+2330A= NP_001128634.1:n.-92+2330A=
NM_001362828.1:c.-385-7215A= NP_001349757.1:n.-385-7215A=
NM_001362828.2:c.-385-7215A= NP_001349757.1:n.-385-7215A=
ENST00000207636.9:c.-92+2932A= ENSP00000207636.5:n.-92+2932A=
ENST00000361682.10:c.-91-7215A= ENSP00000354511.6:n.-91-7215A=
ENST00000403184.5:c.-91-7215A= ENSP00000383966.1:n.-91-7215A=
ENST00000403710.5:c.-385-7215A= ENSP00000385917.1:n.-385-7215A=
ENST00000406520.7:c.-92+2330A= ENSP00000385150.3:n.-92+2330A=
ENST00000407537.5:c.-269-7215A= ENSP00000384654.2:n.-269-7215A=
ENST00000412786.5:c.-92+2932A= ENSP00000403958.1:n.-92+2932A=
ENST00000428707.2:c.-91-7215A= ENSP00000387695.2:n.-91-7215A=
ENST00000467943.5:n.106-7215A=
ENST00000676678.1:c.-91-7215A= ENSP00000503719.1:n.-91-7215A=
ENST00000678255.1:c.-922+35A= ENSP00000504402.1:n.-922+35A=
ENST00000678769.1:c.-91-7215A= ENSP00000503289.1:n.-91-7215A=
ENST00000678868.1:c.-92+6494A= ENSP00000503583.1:n.-92+6494A=
XM_011529887.1:c.-91-7215A= XP_011528189.1:n.-91-7215A=
XM_011529888.1:c.-92+2330A= XP_011528190.1:n.-92+2330A=
XM_011529889.1:c.-92+2932A= XP_011528191.1:n.-92+2932A=
XM_011529890.1:c.-385-7215A= XP_011528192.1:n.-385-7215A=
XM_011529891.1:c.-385-7215A= XP_011528193.1:n.-385-7215A=
XM_017028595.1:c.-385-7215A= XP_016884084.1:n.-385-7215A=