Canonical Allele Identifier: CA2396122705

Gene: COMT

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19957504_19957506delinsACT , CM000684.2:g.19957504_19957506delinsACT	GRCh38
NC_000022.10:g.19945027_19945029delinsACT , CM000684.1:g.19945027_19945029delinsACT	GRCh37
NC_000022.9:g.18325027_18325029delinsACT	NCBI36
NG_011526.1:g.20765_20767delinsACT

Transcript Alleles

HGVS	Amino-acid change
ENST00000361682.11:c.-91-3695_-91-3693delinsACT MANE Select	ENSP00000354511.6:n.-91-3695_-91-3693deli...
ENST00000428707.2:c.-91-3695_-91-3693delinsACT	ENSP00000387695.2:n.-91-3695_-91-3693deli...
ENST00000676678.1:c.-91-3695_-91-3693delinsACT	ENSP00000503719.1:n.-91-3695_-91-3693deli...
ENST00000678255.1:c.-922+3555_-922+3557delinsACT	ENSP00000504402.1:n.-922+3555_-922+3557de...
ENST00000678769.1:c.-91-3695_-91-3693delinsACT	ENSP00000503289.1:n.-91-3695_-91-3693deli...
ENST00000678868.1:c.-91-3695_-91-3693delinsACT	ENSP00000503583.1:n.-91-3695_-91-3693deli...
ENST00000207636.9:c.-91-3695_-91-3693delinsACT	ENSP00000207636.5:n.-91-3695_-91-3693deli...
ENST00000361682.10:c.-91-3695_-91-3693delinsACT	ENSP00000354511.6:n.-91-3695_-91-3693deli...
ENST00000403184.5:c.-91-3695_-91-3693delinsACT	ENSP00000383966.1:n.-91-3695_-91-3693deli...
ENST00000403710.5:c.-385-3695_-385-3693delinsACT	ENSP00000385917.1:n.-385-3695_-385-3693de...
ENST00000406520.7:c.-91-3695_-91-3693delinsACT	ENSP00000385150.3:n.-91-3695_-91-3693deli...
ENST00000407537.5:c.-269-3695_-269-3693delinsACT	ENSP00000384654.2:n.-269-3695_-269-3693de...
ENST00000412786.5:c.-91-3695_-91-3693delinsACT	ENSP00000403958.1:n.-91-3695_-91-3693deli...
ENST00000467943.5:n.106-3695_106-3693delinsACT
NM_000754.3:c.-91-3695_-91-3693delinsACT	NP_000745.1:n.-91-3695_-91-3693delinsACT
NM_001135161.1:c.-91-3695_-91-3693delinsACT	NP_001128633.1:n.-91-3695_-91-3693delinsA...
NM_001135162.1:c.-91-3695_-91-3693delinsACT	NP_001128634.1:n.-91-3695_-91-3693delinsA...
XM_011529887.1:c.-91-3695_-91-3693delinsACT	XP_011528189.1:n.-91-3695_-91-3693delinsA...
XM_011529888.1:c.-91-3695_-91-3693delinsACT	XP_011528190.1:n.-91-3695_-91-3693delinsA...
XM_011529889.1:c.-91-3695_-91-3693delinsACT	XP_011528191.1:n.-91-3695_-91-3693delinsA...
XM_011529890.1:c.-385-3695_-385-3693delinsACT	XP_011528192.1:n.-385-3695_-385-3693delin...
XM_011529891.1:c.-385-3695_-385-3693delinsACT	XP_011528193.1:n.-385-3695_-385-3693delin...
NM_001362828.1:c.-385-3695_-385-3693delinsACT	NP_001349757.1:n.-385-3695_-385-3693delin...
XM_011529886.2:c.-184_-182delinsACT	XP_011528188.2:n.-184_-182delinsACT
XM_017028595.1:c.-385-3695_-385-3693delinsACT	XP_016884084.1:n.-385-3695_-385-3693delin...
NM_000754.4:c.-91-3695_-91-3693delinsACT MANE Select	NP_000745.1:n.-91-3695_-91-3693delinsACT
NM_001135161.2:c.-91-3695_-91-3693delinsACT	NP_001128633.1:n.-91-3695_-91-3693delinsA...
NM_001135162.2:c.-91-3695_-91-3693delinsACT	NP_001128634.1:n.-91-3695_-91-3693delinsA...
NM_001362828.2:c.-385-3695_-385-3693delinsACT	NP_001349757.1:n.-385-3695_-385-3693delin...