Canonical Allele Identifier: CA2396126037

Gene: COMT

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19964133_19964134delinsTG , CM000684.2:g.19964133_19964134delinsTG	GRCh38
NC_000022.10:g.19951656_19951657delinsTG , CM000684.1:g.19951656_19951657delinsTG	GRCh37
NC_000022.9:g.18331656_18331657delinsTG	NCBI36
NG_011526.1:g.27394_27395delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361682.11:c.484-35_484-34delinsTG MANE Select	ENSP00000354511.6:n.484-35_484-34delinsTG
ENST00000428707.2:c.484-35_484-34delinsTG	ENSP00000387695.2:n.484-35_484-34delinsTG
ENST00000676678.1:c.484-35_484-34delinsTG	ENSP00000503719.1:n.484-35_484-34delinsTG
ENST00000677397.1:c.334-35_334-34delinsTG	ENSP00000503422.1:n.334-35_334-34delinsTG
ENST00000677470.1:n.299_300delinsTG
ENST00000677564.1:n.267-35_267-34delinsTG
ENST00000677675.1:n.284-35_284-34delinsTG
ENST00000678240.1:n.332-35_332-34delinsTG
ENST00000678255.1:c.484-35_484-34delinsTG	ENSP00000504402.1:n.484-35_484-34delinsTG
ENST00000678769.1:c.484-35_484-34delinsTG	ENSP00000503289.1:n.484-35_484-34delinsTG
ENST00000678868.1:c.484-35_484-34delinsTG	ENSP00000503583.1:n.484-35_484-34delinsTG
ENST00000678945.1:n.317_318delinsTG
ENST00000207636.9:c.507_508delinsTG	ENSP00000207636.5:p.Ser169=
ENST00000361682.10:c.484-35_484-34delinsTG	ENSP00000354511.6:n.484-35_484-34delinsTG
ENST00000403184.5:c.484-35_484-34delinsTG	ENSP00000383966.1:n.484-35_484-34delinsTG
ENST00000403710.5:c.484-35_484-34delinsTG	ENSP00000385917.1:n.484-35_484-34delinsTG
ENST00000406520.7:c.484-35_484-34delinsTG	ENSP00000385150.3:n.484-35_484-34delinsTG
ENST00000407537.5:c.484-35_484-34delinsTG	ENSP00000384654.2:n.484-35_484-34delinsTG
ENST00000412786.5:c.484-35_484-34delinsTG	ENSP00000403958.1:n.484-35_484-34delinsTG
ENST00000428707.1:c.62-35_62-34delinsTG
ENST00000449653.5:c.334-35_334-34delinsTG	ENSP00000416778.1:n.334-35_334-34delinsTG
ENST00000493893.1:n.222-35_222-34delinsTG
NM_000754.3:c.484-35_484-34delinsTG	NP_000745.1:n.484-35_484-34delinsTG
NM_001135161.1:c.484-35_484-34delinsTG	NP_001128633.1:n.484-35_484-34delinsTG
NM_001135162.1:c.484-35_484-34delinsTG	NP_001128634.1:n.484-35_484-34delinsTG
NM_007310.2:c.334-35_334-34delinsTG	NP_009294.1:n.334-35_334-34delinsTG
XM_011529885.1:c.598-35_598-34delinsTG	XP_011528187.1:n.598-35_598-34delinsTG
XM_011529886.1:c.598-35_598-34delinsTG	XP_011528188.1:n.598-35_598-34delinsTG
XM_011529887.1:c.484-35_484-34delinsTG	XP_011528189.1:n.484-35_484-34delinsTG
XM_011529888.1:c.484-35_484-34delinsTG	XP_011528190.1:n.484-35_484-34delinsTG
XM_011529889.1:c.484-35_484-34delinsTG	XP_011528191.1:n.484-35_484-34delinsTG
XM_011529890.1:c.484-35_484-34delinsTG	XP_011528192.1:n.484-35_484-34delinsTG
XM_011529891.1:c.484-35_484-34delinsTG	XP_011528193.1:n.484-35_484-34delinsTG
NM_001362828.1:c.484-35_484-34delinsTG	NP_001349757.1:n.484-35_484-34delinsTG
XM_011529886.2:c.895-35_895-34delinsTG	XP_011528188.2:n.895-35_895-34delinsTG
XM_017028595.1:c.484-35_484-34delinsTG	XP_016884084.1:n.484-35_484-34delinsTG
NM_000754.4:c.484-35_484-34delinsTG MANE Select	NP_000745.1:n.484-35_484-34delinsTG
NM_001135161.2:c.484-35_484-34delinsTG	NP_001128633.1:n.484-35_484-34delinsTG
NM_001135162.2:c.484-35_484-34delinsTG	NP_001128634.1:n.484-35_484-34delinsTG
NM_001362828.2:c.484-35_484-34delinsTG	NP_001349757.1:n.484-35_484-34delinsTG
NM_007310.3:c.334-35_334-34delinsTG	NP_009294.1:n.334-35_334-34delinsTG