Canonical Allele Identifier: CA2818396478

Gene: COMT

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19942597dup , CM000684.2:g.19942597dup	GRCh38
NC_000022.10:g.19930120dup , CM000684.1:g.19930120dup	GRCh37
NC_000022.9:g.18310120dup	NCBI36
NG_011526.1:g.5858dup
NG_011835.1:g.4242dup , LRG_417:g.4242dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361682.11:c.-92+700dup MANE Select	ENSP00000354511.6:n.-92+700dup
ENST00000428707.2:c.-92+700dup	ENSP00000387695.2:n.-92+700dup
ENST00000676678.1:c.-92+1022dup	ENSP00000503719.1:n.-92+1022dup
ENST00000678769.1:c.-92+700dup	ENSP00000503289.1:n.-92+700dup
ENST00000678868.1:c.-276+700dup	ENSP00000503583.1:n.-276+700dup
ENST00000361682.10:c.-92+700dup	ENSP00000354511.6:n.-92+700dup
ENST00000403184.5:c.-92+700dup	ENSP00000383966.1:n.-92+700dup
ENST00000403710.5:c.-386+700dup	ENSP00000385917.1:n.-386+700dup
ENST00000407537.5:c.-270+700dup	ENSP00000384654.2:n.-270+700dup
ENST00000467943.5:n.105+700dup
NM_000754.3:c.-92+700dup	NP_000745.1:n.-92+700dup
XM_011529887.1:c.-92+700dup	XP_011528189.1:n.-92+700dup
XM_011529890.1:c.-386+700dup	XP_011528192.1:n.-386+700dup
XM_011529891.1:c.-386+422dup	XP_011528193.1:n.-386+422dup
NM_001362828.1:c.-386+700dup	NP_001349757.1:n.-386+700dup
XM_017028595.1:c.-386+422dup	XP_016884084.1:n.-386+422dup
NM_000754.4:c.-92+700dup MANE Select	NP_000745.1:n.-92+700dup
NM_001362828.2:c.-386+700dup	NP_001349757.1:n.-386+700dup