Canonical Allele Identifier: CA2396125997

Gene: COMT

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19964067_19964071delinsCCTGT , CM000684.2:g.19964067_19964071delinsCCTGT	GRCh38
NC_000022.10:g.19951590_19951594delinsCCTGT , CM000684.1:g.19951590_19951594delinsCCTGT	GRCh37
NC_000022.9:g.18331590_18331594delinsCCTGT	NCBI36
NG_011526.1:g.27328_27332delinsCCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361682.11:c.484-101_484-97delinsCCTGT MANE Select	ENSP00000354511.6:n.484-101_484-97delinsCCTGT
ENST00000428707.2:c.484-101_484-97delinsCCTGT	ENSP00000387695.2:n.484-101_484-97delinsCCTGT
ENST00000676678.1:c.484-101_484-97delinsCCTGT	ENSP00000503719.1:n.484-101_484-97delinsCCTGT
ENST00000677397.1:c.334-101_334-97delinsCCTGT	ENSP00000503422.1:n.334-101_334-97delinsCCTGT
ENST00000677470.1:n.233_237delinsCCTGT
ENST00000677564.1:n.267-101_267-97delinsCCTGT
ENST00000677675.1:n.284-101_284-97delinsCCTGT
ENST00000678240.1:n.332-101_332-97delinsCCTGT
ENST00000678255.1:c.484-101_484-97delinsCCTGT	ENSP00000504402.1:n.484-101_484-97delinsCCTGT
ENST00000678769.1:c.484-101_484-97delinsCCTGT	ENSP00000503289.1:n.484-101_484-97delinsCCTGT
ENST00000678868.1:c.484-101_484-97delinsCCTGT	ENSP00000503583.1:n.484-101_484-97delinsCCTGT
ENST00000678945.1:n.294-43_294-39delinsCCTGT
ENST00000207636.9:c.484-43_484-39delinsCCTGT	ENSP00000207636.5:n.484-43_484-39delinsCCTGT
ENST00000361682.10:c.484-101_484-97delinsCCTGT	ENSP00000354511.6:n.484-101_484-97delinsCCTGT
ENST00000403184.5:c.484-101_484-97delinsCCTGT	ENSP00000383966.1:n.484-101_484-97delinsCCTGT
ENST00000403710.5:c.484-101_484-97delinsCCTGT	ENSP00000385917.1:n.484-101_484-97delinsCCTGT
ENST00000406520.7:c.484-101_484-97delinsCCTGT	ENSP00000385150.3:n.484-101_484-97delinsCCTGT
ENST00000407537.5:c.484-101_484-97delinsCCTGT	ENSP00000384654.2:n.484-101_484-97delinsCCTGT
ENST00000412786.5:c.484-101_484-97delinsCCTGT	ENSP00000403958.1:n.484-101_484-97delinsCCTGT
ENST00000428707.1:c.62-101_62-97delinsCCTGT
ENST00000449653.5:c.334-101_334-97delinsCCTGT	ENSP00000416778.1:n.334-101_334-97delinsCCTGT
ENST00000493893.1:n.222-101_222-97delinsCCTGT
NM_000754.3:c.484-101_484-97delinsCCTGT	NP_000745.1:n.484-101_484-97delinsCCTGT
NM_001135161.1:c.484-101_484-97delinsCCTGT	NP_001128633.1:n.484-101_484-97delinsCCTGT
NM_001135162.1:c.484-101_484-97delinsCCTGT	NP_001128634.1:n.484-101_484-97delinsCCTGT
NM_007310.2:c.334-101_334-97delinsCCTGT	NP_009294.1:n.334-101_334-97delinsCCTGT
XM_011529885.1:c.598-101_598-97delinsCCTGT	XP_011528187.1:n.598-101_598-97delinsCCTGT
XM_011529886.1:c.598-101_598-97delinsCCTGT	XP_011528188.1:n.598-101_598-97delinsCCTGT
XM_011529887.1:c.484-101_484-97delinsCCTGT	XP_011528189.1:n.484-101_484-97delinsCCTGT
XM_011529888.1:c.484-101_484-97delinsCCTGT	XP_011528190.1:n.484-101_484-97delinsCCTGT
XM_011529889.1:c.484-101_484-97delinsCCTGT	XP_011528191.1:n.484-101_484-97delinsCCTGT
XM_011529890.1:c.484-101_484-97delinsCCTGT	XP_011528192.1:n.484-101_484-97delinsCCTGT
XM_011529891.1:c.484-101_484-97delinsCCTGT	XP_011528193.1:n.484-101_484-97delinsCCTGT
NM_001362828.1:c.484-101_484-97delinsCCTGT	NP_001349757.1:n.484-101_484-97delinsCCTGT
XM_011529886.2:c.895-101_895-97delinsCCTGT	XP_011528188.2:n.895-101_895-97delinsCCTGT
XM_017028595.1:c.484-101_484-97delinsCCTGT	XP_016884084.1:n.484-101_484-97delinsCCTGT
NM_000754.4:c.484-101_484-97delinsCCTGT MANE Select	NP_000745.1:n.484-101_484-97delinsCCTGT
NM_001135161.2:c.484-101_484-97delinsCCTGT	NP_001128633.1:n.484-101_484-97delinsCCTGT
NM_001135162.2:c.484-101_484-97delinsCCTGT	NP_001128634.1:n.484-101_484-97delinsCCTGT
NM_001362828.2:c.484-101_484-97delinsCCTGT	NP_001349757.1:n.484-101_484-97delinsCCTGT
NM_007310.3:c.334-101_334-97delinsCCTGT	NP_009294.1:n.334-101_334-97delinsCCTGT