Canonical Allele Identifier: CA2396122625

Gene: COMT

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19957314_19957317delinsACTC , CM000684.2:g.19957314_19957317delinsACTC	GRCh38
NC_000022.10:g.19944837_19944840delinsACTC , CM000684.1:g.19944837_19944840delinsACTC	GRCh37
NC_000022.9:g.18324837_18324840delinsACTC	NCBI36
NG_011526.1:g.20575_20578delinsACTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361682.11:c.-91-3885_-91-3882delinsACTC MANE Select	ENSP00000354511.6:n.-91-3885_-91-3882delinsACTC
ENST00000428707.2:c.-91-3885_-91-3882delinsACTC	ENSP00000387695.2:n.-91-3885_-91-3882delinsACTC
ENST00000676678.1:c.-91-3885_-91-3882delinsACTC	ENSP00000503719.1:n.-91-3885_-91-3882delinsACTC
ENST00000678255.1:c.-922+3365_-922+3368delinsACTC	ENSP00000504402.1:n.-922+3365_-922+3368delinsACTC
ENST00000678769.1:c.-91-3885_-91-3882delinsACTC	ENSP00000503289.1:n.-91-3885_-91-3882delinsACTC
ENST00000678868.1:c.-91-3885_-91-3882delinsACTC	ENSP00000503583.1:n.-91-3885_-91-3882delinsACTC
ENST00000207636.9:c.-91-3885_-91-3882delinsACTC	ENSP00000207636.5:n.-91-3885_-91-3882delinsACTC
ENST00000361682.10:c.-91-3885_-91-3882delinsACTC	ENSP00000354511.6:n.-91-3885_-91-3882delinsACTC
ENST00000403184.5:c.-91-3885_-91-3882delinsACTC	ENSP00000383966.1:n.-91-3885_-91-3882delinsACTC
ENST00000403710.5:c.-385-3885_-385-3882delinsACTC	ENSP00000385917.1:n.-385-3885_-385-3882delinsACTC
ENST00000406520.7:c.-91-3885_-91-3882delinsACTC	ENSP00000385150.3:n.-91-3885_-91-3882delinsACTC
ENST00000407537.5:c.-269-3885_-269-3882delinsACTC	ENSP00000384654.2:n.-269-3885_-269-3882delinsACTC
ENST00000412786.5:c.-91-3885_-91-3882delinsACTC	ENSP00000403958.1:n.-91-3885_-91-3882delinsACTC
ENST00000467943.5:n.106-3885_106-3882delinsACTC
NM_000754.3:c.-91-3885_-91-3882delinsACTC	NP_000745.1:n.-91-3885_-91-3882delinsACTC
NM_001135161.1:c.-91-3885_-91-3882delinsACTC	NP_001128633.1:n.-91-3885_-91-3882delinsACTC
NM_001135162.1:c.-91-3885_-91-3882delinsACTC	NP_001128634.1:n.-91-3885_-91-3882delinsACTC
XM_011529887.1:c.-91-3885_-91-3882delinsACTC	XP_011528189.1:n.-91-3885_-91-3882delinsACTC
XM_011529888.1:c.-91-3885_-91-3882delinsACTC	XP_011528190.1:n.-91-3885_-91-3882delinsACTC
XM_011529889.1:c.-91-3885_-91-3882delinsACTC	XP_011528191.1:n.-91-3885_-91-3882delinsACTC
XM_011529890.1:c.-385-3885_-385-3882delinsACTC	XP_011528192.1:n.-385-3885_-385-3882delinsACTC
XM_011529891.1:c.-385-3885_-385-3882delinsACTC	XP_011528193.1:n.-385-3885_-385-3882delinsACTC
NM_001362828.1:c.-385-3885_-385-3882delinsACTC	NP_001349757.1:n.-385-3885_-385-3882delinsACTC
XM_011529886.2:c.-374_-371delinsACTC	XP_011528188.2:n.-374_-371delinsACTC
XM_017028595.1:c.-385-3885_-385-3882delinsACTC	XP_016884084.1:n.-385-3885_-385-3882delinsACTC
NM_000754.4:c.-91-3885_-91-3882delinsACTC MANE Select	NP_000745.1:n.-91-3885_-91-3882delinsACTC
NM_001135161.2:c.-91-3885_-91-3882delinsACTC	NP_001128633.1:n.-91-3885_-91-3882delinsACTC
NM_001135162.2:c.-91-3885_-91-3882delinsACTC	NP_001128634.1:n.-91-3885_-91-3882delinsACTC
NM_001362828.2:c.-385-3885_-385-3882delinsACTC	NP_001349757.1:n.-385-3885_-385-3882delinsACTC