Canonical Allele Identifier: CA2396124388

Gene: COMT

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19960761_19960765delinsCCTAT , CM000684.2:g.19960761_19960765delinsCCTAT	GRCh38
NC_000022.10:g.19948284_19948288delinsCCTAT , CM000684.1:g.19948284_19948288delinsCCTAT	GRCh37
NC_000022.9:g.18328284_18328288delinsCCTAT	NCBI36
NG_011526.1:g.24022_24026delinsCCTAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000361682.11:c.-91-438_-91-434delinsCCTAT MANE Select	ENSP00000354511.6:n.-91-438_-91-434delins...
ENST00000428707.2:c.-91-438_-91-434delinsCCTAT	ENSP00000387695.2:n.-91-438_-91-434delins...
ENST00000676678.1:c.-91-438_-91-434delinsCCTAT	ENSP00000503719.1:n.-91-438_-91-434delins...
ENST00000678255.1:c.-921-438_-921-434delinsCCTAT	ENSP00000504402.1:n.-921-438_-921-434deli...
ENST00000678769.1:c.-91-438_-91-434delinsCCTAT	ENSP00000503289.1:n.-91-438_-91-434delins...
ENST00000678868.1:c.-91-438_-91-434delinsCCTAT	ENSP00000503583.1:n.-91-438_-91-434delins...
ENST00000207636.9:c.-91-438_-91-434delinsCCTAT	ENSP00000207636.5:n.-91-438_-91-434delins...
ENST00000361682.10:c.-91-438_-91-434delinsCCTAT	ENSP00000354511.6:n.-91-438_-91-434delins...
ENST00000403184.5:c.-91-438_-91-434delinsCCTAT	ENSP00000383966.1:n.-91-438_-91-434delins...
ENST00000403710.5:c.-385-438_-385-434delinsCCTAT	ENSP00000385917.1:n.-385-438_-385-434deli...
ENST00000406520.7:c.-91-438_-91-434delinsCCTAT	ENSP00000385150.3:n.-91-438_-91-434delins...
ENST00000407537.5:c.-269-438_-269-434delinsCCTAT	ENSP00000384654.2:n.-269-438_-269-434deli...
ENST00000412786.5:c.-91-438_-91-434delinsCCTAT	ENSP00000403958.1:n.-91-438_-91-434delins...
ENST00000467943.5:n.106-438_106-434delinsCCTAT
NM_000754.3:c.-91-438_-91-434delinsCCTAT	NP_000745.1:n.-91-438_-91-434delinsCCTAT
NM_001135161.1:c.-91-438_-91-434delinsCCTAT	NP_001128633.1:n.-91-438_-91-434delinsCCT...
NM_001135162.1:c.-91-438_-91-434delinsCCTAT	NP_001128634.1:n.-91-438_-91-434delinsCCT...
XM_011529885.1:c.24-438_24-434delinsCCTAT	XP_011528187.1:n.24-438_24-434delinsCCTAT...
XM_011529886.1:c.24-438_24-434delinsCCTAT	XP_011528188.1:n.24-438_24-434delinsCCTAT...
XM_011529887.1:c.-91-438_-91-434delinsCCTAT	XP_011528189.1:n.-91-438_-91-434delinsCCT...
XM_011529888.1:c.-91-438_-91-434delinsCCTAT	XP_011528190.1:n.-91-438_-91-434delinsCCT...
XM_011529889.1:c.-91-438_-91-434delinsCCTAT	XP_011528191.1:n.-91-438_-91-434delinsCCT...
XM_011529890.1:c.-385-438_-385-434delinsCCTAT	XP_011528192.1:n.-385-438_-385-434delinsC...
XM_011529891.1:c.-385-438_-385-434delinsCCTAT	XP_011528193.1:n.-385-438_-385-434delinsC...
NM_001362828.1:c.-385-438_-385-434delinsCCTAT	NP_001349757.1:n.-385-438_-385-434delinsC...
XM_011529886.2:c.321-438_321-434delinsCCTAT	XP_011528188.2:n.321-438_321-434delinsCCT...
XM_017028595.1:c.-385-438_-385-434delinsCCTAT	XP_016884084.1:n.-385-438_-385-434delinsC...
NM_000754.4:c.-91-438_-91-434delinsCCTAT MANE Select	NP_000745.1:n.-91-438_-91-434delinsCCTAT
NM_001135161.2:c.-91-438_-91-434delinsCCTAT	NP_001128633.1:n.-91-438_-91-434delinsCCT...
NM_001135162.2:c.-91-438_-91-434delinsCCTAT	NP_001128634.1:n.-91-438_-91-434delinsCCT...
NM_001362828.2:c.-385-438_-385-434delinsCCTAT	NP_001349757.1:n.-385-438_-385-434delinsC...