Canonical Allele Identifier: CA2396116185
Gene: COMT HGNC NCBI

Linked Data

dbSNP Id: rs1941788479

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19943741_19943742insTTTTTGA , CM000684.2:g.19943741_19943742insTTTTTGA GRCh38
NC_000022.10:g.19931264_19931265insTTTTTGA , CM000684.1:g.19931264_19931265insTTTTTGA GRCh37
NC_000022.9:g.18311264_18311265insTTTTTGA NCBI36
NG_011526.1:g.7002_7003insTTTTTGA
NG_011835.1:g.3095_3096insTCAAAAA , LRG_417:g.3095_3096insTCAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000361682.11:c.-92+1844_-92+1845insTTTTTGA MANE Select ENSP00000354511.6:n.-92+1844_-92+1845insTTTTTGA
ENST00000428707.2:c.-92+1844_-92+1845insTTTTTGA ENSP00000387695.2:n.-92+1844_-92+1845insTTTTTGA
ENST00000676678.1:c.-92+2166_-92+2167insTTTTTGA ENSP00000503719.1:n.-92+2166_-92+2167insTTTTTGA
ENST00000678769.1:c.-92+1844_-92+1845insTTTTTGA ENSP00000503289.1:n.-92+1844_-92+1845insTTTTTGA
ENST00000678868.1:c.-276+1844_-276+1845insTTTTTGA ENSP00000503583.1:n.-276+1844_-276+1845insTTTTTGA
ENST00000361682.10:c.-92+1844_-92+1845insTTTTTGA ENSP00000354511.6:n.-92+1844_-92+1845insTTTTTGA
ENST00000403184.5:c.-92+1844_-92+1845insTTTTTGA ENSP00000383966.1:n.-92+1844_-92+1845insTTTTTGA
ENST00000403710.5:c.-386+1844_-386+1845insTTTTTGA ENSP00000385917.1:n.-386+1844_-386+1845insTTTTTGA
ENST00000407537.5:c.-270+1844_-270+1845insTTTTTGA ENSP00000384654.2:n.-270+1844_-270+1845insTTTTTGA
ENST00000467943.5:n.105+1844_105+1845insTTTTTGA
NM_000754.3:c.-92+1844_-92+1845insTTTTTGA NP_000745.1:n.-92+1844_-92+1845insTTTTTGA
XM_011529887.1:c.-92+1844_-92+1845insTTTTTGA XP_011528189.1:n.-92+1844_-92+1845insTTTTTGA
XM_011529890.1:c.-386+1844_-386+1845insTTTTTGA XP_011528192.1:n.-386+1844_-386+1845insTTTTTGA
XM_011529891.1:c.-386+1566_-386+1567insTTTTTGA XP_011528193.1:n.-386+1566_-386+1567insTTTTTGA
NM_001362828.1:c.-386+1844_-386+1845insTTTTTGA NP_001349757.1:n.-386+1844_-386+1845insTTTTTGA
XM_017028595.1:c.-386+1566_-386+1567insTTTTTGA XP_016884084.1:n.-386+1566_-386+1567insTTTTTGA
NM_000754.4:c.-92+1844_-92+1845insTTTTTGA MANE Select NP_000745.1:n.-92+1844_-92+1845insTTTTTGA
NM_001362828.2:c.-386+1844_-386+1845insTTTTTGA NP_001349757.1:n.-386+1844_-386+1845insTTTTTGA