Canonical Allele Identifier: CA2396115695

Gene: COMT

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19942664_19942665delinsGC , CM000684.2:g.19942664_19942665delinsGC	GRCh38
NC_000022.10:g.19930187_19930188delinsGC , CM000684.1:g.19930187_19930188delinsGC	GRCh37
NC_000022.9:g.18310187_18310188delinsGC	NCBI36
NG_011526.1:g.5925_5926delinsGC
NG_011835.1:g.4172_4173delinsGC , LRG_417:g.4172_4173delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000361682.11:c.-92+767_-92+768delinsGC MANE Select	ENSP00000354511.6:n.-92+767_-92+768delins...
ENST00000428707.2:c.-92+767_-92+768delinsGC	ENSP00000387695.2:n.-92+767_-92+768delins...
ENST00000676678.1:c.-92+1089_-92+1090delinsGC	ENSP00000503719.1:n.-92+1089_-92+1090deli...
ENST00000678769.1:c.-92+767_-92+768delinsGC	ENSP00000503289.1:n.-92+767_-92+768delins...
ENST00000678868.1:c.-276+767_-276+768delinsGC	ENSP00000503583.1:n.-276+767_-276+768deli...
ENST00000361682.10:c.-92+767_-92+768delinsGC	ENSP00000354511.6:n.-92+767_-92+768delins...
ENST00000403184.5:c.-92+767_-92+768delinsGC	ENSP00000383966.1:n.-92+767_-92+768delins...
ENST00000403710.5:c.-386+767_-386+768delinsGC	ENSP00000385917.1:n.-386+767_-386+768deli...
ENST00000407537.5:c.-270+767_-270+768delinsGC	ENSP00000384654.2:n.-270+767_-270+768deli...
ENST00000467943.5:n.105+767_105+768delinsGC
NM_000754.3:c.-92+767_-92+768delinsGC	NP_000745.1:n.-92+767_-92+768delinsGC
XM_011529887.1:c.-92+767_-92+768delinsGC	XP_011528189.1:n.-92+767_-92+768delinsGC
XM_011529890.1:c.-386+767_-386+768delinsGC	XP_011528192.1:n.-386+767_-386+768delinsG...
XM_011529891.1:c.-386+489_-386+490delinsGC	XP_011528193.1:n.-386+489_-386+490delinsG...
NM_001362828.1:c.-386+767_-386+768delinsGC	NP_001349757.1:n.-386+767_-386+768delinsG...
XM_017028595.1:c.-386+489_-386+490delinsGC	XP_016884084.1:n.-386+489_-386+490delinsG...
NM_000754.4:c.-92+767_-92+768delinsGC MANE Select	NP_000745.1:n.-92+767_-92+768delinsGC
NM_001362828.2:c.-386+767_-386+768delinsGC	NP_001349757.1:n.-386+767_-386+768delinsG...