Canonical Allele Identifier: CA2396118895
Gene: COMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19949988G= , CM000684.2:g.19949988G= GRCh38
NC_000022.10:g.19937511G= , CM000684.1:g.19937511G= GRCh37
NC_000022.9:g.18317511G= NCBI36
NG_011526.1:g.13249G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361682.11:c.-92+8091G= MANE Select ENSP00000354511.6:n.-92+8091G=
ENST00000428707.2:c.-92+8091G= ENSP00000387695.2:n.-92+8091G=
ENST00000676678.1:c.-92+8413G= ENSP00000503719.1:n.-92+8413G=
ENST00000678769.1:c.-92+8091G= ENSP00000503289.1:n.-92+8091G=
ENST00000678868.1:c.-92+2498G= ENSP00000503583.1:n.-92+2498G=
ENST00000361682.10:c.-92+8091G= ENSP00000354511.6:n.-92+8091G=
ENST00000403184.5:c.-92+8091G= ENSP00000383966.1:n.-92+8091G=
ENST00000403710.5:c.-386+8091G= ENSP00000385917.1:n.-386+8091G=
ENST00000407537.5:c.-270+8091G= ENSP00000384654.2:n.-270+8091G=
ENST00000467943.5:n.105+8091G=
NM_000754.3:c.-92+8091G= NP_000745.1:n.-92+8091G=
XM_011529887.1:c.-92+8091G= XP_011528189.1:n.-92+8091G=
XM_011529890.1:c.-386+8091G= XP_011528192.1:n.-386+8091G=
XM_011529891.1:c.-386+7813G= XP_011528193.1:n.-386+7813G=
NM_001362828.1:c.-386+8091G= NP_001349757.1:n.-386+8091G=
XM_017028595.1:c.-386+7813G= XP_016884084.1:n.-386+7813G=
NM_000754.4:c.-92+8091G= MANE Select NP_000745.1:n.-92+8091G=
NM_001362828.2:c.-386+8091G= NP_001349757.1:n.-386+8091G=