Canonical Allele Identifier: CA2396126120

Gene: COMT

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19964279_19964281delinsCCG , CM000684.2:g.19964279_19964281delinsCCG	GRCh38
NC_000022.10:g.19951802_19951804delinsCCG , CM000684.1:g.19951802_19951804delinsCCG	GRCh37
NC_000022.9:g.18331802_18331804delinsCCG	NCBI36
NG_011526.1:g.27540_27542delinsCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361682.11:c.595_597delinsCCG MANE Select	ENSP00000354511.6:p.Pro199=
ENST00000428707.2:c.595_597delinsCCG	ENSP00000387695.2:p.Pro199=
ENST00000676678.1:c.595_597delinsCCG	ENSP00000503719.1:p.Pro199=
ENST00000677397.1:c.445_447delinsCCG	ENSP00000503422.1:p.Pro149=
ENST00000677470.1:n.445_447delinsCCG
ENST00000677564.1:n.378_380delinsCCG
ENST00000677675.1:n.395_397delinsCCG
ENST00000678240.1:n.443_445delinsCCG
ENST00000678255.1:c.595_597delinsCCG	ENSP00000504402.1:p.Pro199=
ENST00000678769.1:c.595_597delinsCCG	ENSP00000503289.1:p.Pro199=
ENST00000678868.1:c.595_597delinsCCG	ENSP00000503583.1:p.Pro199=
ENST00000678945.1:n.463_465delinsCCG
ENST00000207636.9:c.*53_*55delinsCCG	ENSP00000207636.5:n.*53_*55delinsCCG
ENST00000361682.10:c.595_597delinsCCG	ENSP00000354511.6:p.Pro199=
ENST00000403184.5:c.595_597delinsCCG	ENSP00000383966.1:p.Pro199=
ENST00000403710.5:c.595_597delinsCCG	ENSP00000385917.1:p.Pro199=
ENST00000406520.7:c.595_597delinsCCG	ENSP00000385150.3:p.Pro199=
ENST00000407537.5:c.595_597delinsCCG	ENSP00000384654.2:p.Pro199=
ENST00000412786.5:c.595_597delinsCCG	ENSP00000403958.1:p.Pro199=
ENST00000428707.1:c.173_175delinsCCG
ENST00000449653.5:c.445_447delinsCCG	ENSP00000416778.1:p.Pro149=
ENST00000493893.1:n.333_335delinsCCG
NM_000754.3:c.595_597delinsCCG	NP_000745.1:p.Pro199=
NM_001135161.1:c.595_597delinsCCG	NP_001128633.1:p.Pro199=
NM_001135162.1:c.595_597delinsCCG	NP_001128634.1:p.Pro199=
NM_007310.2:c.445_447delinsCCG	NP_009294.1:p.Pro149=
XM_011529885.1:c.709_711delinsCCG	XP_011528187.1:p.Pro237=
XM_011529886.1:c.709_711delinsCCG	XP_011528188.1:p.Pro237=
XM_011529887.1:c.595_597delinsCCG	XP_011528189.1:p.Pro199=
XM_011529888.1:c.595_597delinsCCG	XP_011528190.1:p.Pro199=
XM_011529889.1:c.595_597delinsCCG	XP_011528191.1:p.Pro199=
XM_011529890.1:c.595_597delinsCCG	XP_011528192.1:p.Pro199=
XM_011529891.1:c.595_597delinsCCG	XP_011528193.1:p.Pro199=
NM_001362828.1:c.595_597delinsCCG	NP_001349757.1:p.Pro199=
XM_011529886.2:c.1006_1008delinsCCG	XP_011528188.2:p.Pro336=
XM_017028595.1:c.595_597delinsCCG	XP_016884084.1:p.Pro199=
NM_000754.4:c.595_597delinsCCG MANE Select	NP_000745.1:p.Pro199=
NM_001135161.2:c.595_597delinsCCG	NP_001128633.1:p.Pro199=
NM_001135162.2:c.595_597delinsCCG	NP_001128634.1:p.Pro199=
NM_001362828.2:c.595_597delinsCCG	NP_001349757.1:p.Pro199=
NM_007310.3:c.445_447delinsCCG	NP_009294.1:p.Pro149=