Canonical Allele Identifier: CA2655333939

Gene: COMT

Linked Data

• gnomAD v4: 22-19963875-TATC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19963877_19963879del , CM000684.2:g.19963877_19963879del	GRCh38
NC_000022.10:g.19951400_19951402del , CM000684.1:g.19951400_19951402del	GRCh37
NC_000022.9:g.18331400_18331402del	NCBI36
NG_011526.1:g.27138_27140del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361682.11:c.483+118_483+120del MANE Select	ENSP00000354511.6:n.483+118_483+120del
ENST00000428707.2:c.483+118_483+120del	ENSP00000387695.2:n.483+118_483+120del
ENST00000676678.1:c.483+118_483+120del	ENSP00000503719.1:n.483+118_483+120del
ENST00000677397.1:c.333+118_333+120del	ENSP00000503422.1:n.333+118_333+120del
ENST00000677470.1:n.43_45del
ENST00000677564.1:n.266+118_266+120del
ENST00000677675.1:n.283+118_283+120del
ENST00000678240.1:n.331+118_331+120del
ENST00000678255.1:c.483+118_483+120del	ENSP00000504402.1:n.483+118_483+120del
ENST00000678769.1:c.483+118_483+120del	ENSP00000503289.1:n.483+118_483+120del
ENST00000678868.1:c.483+118_483+120del	ENSP00000503583.1:n.483+118_483+120del
ENST00000678945.1:n.293+118_293+120del
ENST00000207636.9:c.483+118_483+120del	ENSP00000207636.5:n.483+118_483+120del
ENST00000361682.10:c.483+118_483+120del	ENSP00000354511.6:n.483+118_483+120del
ENST00000403184.5:c.483+118_483+120del	ENSP00000383966.1:n.483+118_483+120del
ENST00000403710.5:c.483+118_483+120del	ENSP00000385917.1:n.483+118_483+120del
ENST00000406520.7:c.483+118_483+120del	ENSP00000385150.3:n.483+118_483+120del
ENST00000407537.5:c.483+118_483+120del	ENSP00000384654.2:n.483+118_483+120del
ENST00000412786.5:c.483+118_483+120del	ENSP00000403958.1:n.483+118_483+120del
ENST00000428707.1:c.61+118_61+120del
ENST00000449653.5:c.333+118_333+120del	ENSP00000416778.1:n.333+118_333+120del
ENST00000493893.1:n.221+118_221+120del
NM_000754.3:c.483+118_483+120del	NP_000745.1:n.483+118_483+120del
NM_001135161.1:c.483+118_483+120del	NP_001128633.1:n.483+118_483+120del
NM_001135162.1:c.483+118_483+120del	NP_001128634.1:n.483+118_483+120del
NM_007310.2:c.333+118_333+120del	NP_009294.1:n.333+118_333+120del
XM_011529885.1:c.597+118_597+120del	XP_011528187.1:n.597+118_597+120del
XM_011529886.1:c.597+118_597+120del	XP_011528188.1:n.597+118_597+120del
XM_011529887.1:c.483+118_483+120del	XP_011528189.1:n.483+118_483+120del
XM_011529888.1:c.483+118_483+120del	XP_011528190.1:n.483+118_483+120del
XM_011529889.1:c.483+118_483+120del	XP_011528191.1:n.483+118_483+120del
XM_011529890.1:c.483+118_483+120del	XP_011528192.1:n.483+118_483+120del
XM_011529891.1:c.483+118_483+120del	XP_011528193.1:n.483+118_483+120del
NM_001362828.1:c.483+118_483+120del	NP_001349757.1:n.483+118_483+120del
XM_011529886.2:c.894+118_894+120del	XP_011528188.2:n.894+118_894+120del
XM_017028595.1:c.483+118_483+120del	XP_016884084.1:n.483+118_483+120del
NM_000754.4:c.483+118_483+120del MANE Select	NP_000745.1:n.483+118_483+120del
NM_001135161.2:c.483+118_483+120del	NP_001128633.1:n.483+118_483+120del
NM_001135162.2:c.483+118_483+120del	NP_001128634.1:n.483+118_483+120del
NM_001362828.2:c.483+118_483+120del	NP_001349757.1:n.483+118_483+120del
NM_007310.3:c.333+118_333+120del	NP_009294.1:n.333+118_333+120del