Canonical Allele Identifier: CA2396126118

Gene: COMT

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19964278_19964279delinsGC , CM000684.2:g.19964278_19964279delinsGC	GRCh38
NC_000022.10:g.19951801_19951802delinsGC , CM000684.1:g.19951801_19951802delinsGC	GRCh37
NC_000022.9:g.18331801_18331802delinsGC	NCBI36
NG_011526.1:g.27539_27540delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361682.11:c.594_595delinsGC MANE Select	ENSP00000354511.6:p.Leu198=
ENST00000428707.2:c.594_595delinsGC	ENSP00000387695.2:p.Leu198=
ENST00000676678.1:c.594_595delinsGC	ENSP00000503719.1:p.Leu198=
ENST00000677397.1:c.444_445delinsGC	ENSP00000503422.1:p.Leu148=
ENST00000677470.1:n.444_445delinsGC
ENST00000677564.1:n.377_378delinsGC
ENST00000677675.1:n.394_395delinsGC
ENST00000678240.1:n.442_443delinsGC
ENST00000678255.1:c.594_595delinsGC	ENSP00000504402.1:p.Leu198=
ENST00000678769.1:c.594_595delinsGC	ENSP00000503289.1:p.Leu198=
ENST00000678868.1:c.594_595delinsGC	ENSP00000503583.1:p.Leu198=
ENST00000678945.1:n.462_463delinsGC
ENST00000207636.9:c.*52_*53delinsGC	ENSP00000207636.5:n.*52_*53delinsGC
ENST00000361682.10:c.594_595delinsGC	ENSP00000354511.6:p.Leu198=
ENST00000403184.5:c.594_595delinsGC	ENSP00000383966.1:p.Leu198=
ENST00000403710.5:c.594_595delinsGC	ENSP00000385917.1:p.Leu198=
ENST00000406520.7:c.594_595delinsGC	ENSP00000385150.3:p.Leu198=
ENST00000407537.5:c.594_595delinsGC	ENSP00000384654.2:p.Leu198=
ENST00000412786.5:c.594_595delinsGC	ENSP00000403958.1:p.Leu198=
ENST00000428707.1:c.172_173delinsGC
ENST00000449653.5:c.444_445delinsGC	ENSP00000416778.1:p.Leu148=
ENST00000493893.1:n.332_333delinsGC
NM_000754.3:c.594_595delinsGC	NP_000745.1:p.Leu198=
NM_001135161.1:c.594_595delinsGC	NP_001128633.1:p.Leu198=
NM_001135162.1:c.594_595delinsGC	NP_001128634.1:p.Leu198=
NM_007310.2:c.444_445delinsGC	NP_009294.1:p.Leu148=
XM_011529885.1:c.708_709delinsGC	XP_011528187.1:p.Leu236=
XM_011529886.1:c.708_709delinsGC	XP_011528188.1:p.Leu236=
XM_011529887.1:c.594_595delinsGC	XP_011528189.1:p.Leu198=
XM_011529888.1:c.594_595delinsGC	XP_011528190.1:p.Leu198=
XM_011529889.1:c.594_595delinsGC	XP_011528191.1:p.Leu198=
XM_011529890.1:c.594_595delinsGC	XP_011528192.1:p.Leu198=
XM_011529891.1:c.594_595delinsGC	XP_011528193.1:p.Leu198=
NM_001362828.1:c.594_595delinsGC	NP_001349757.1:p.Leu198=
XM_011529886.2:c.1005_1006delinsGC	XP_011528188.2:p.Leu335=
XM_017028595.1:c.594_595delinsGC	XP_016884084.1:p.Leu198=
NM_000754.4:c.594_595delinsGC MANE Select	NP_000745.1:p.Leu198=
NM_001135161.2:c.594_595delinsGC	NP_001128633.1:p.Leu198=
NM_001135162.2:c.594_595delinsGC	NP_001128634.1:p.Leu198=
NM_001362828.2:c.594_595delinsGC	NP_001349757.1:p.Leu198=
NM_007310.3:c.444_445delinsGC	NP_009294.1:p.Leu148=