Canonical Allele Identifier: CA2396124713

Gene: COMT

Linked Data

• dbSNP Id: rs1942191061

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19961475_19961477del , CM000684.2:g.19961475_19961477del	GRCh38
NC_000022.10:g.19948998_19949000del , CM000684.1:g.19948998_19949000del	GRCh37
NC_000022.9:g.18328998_18329000del	NCBI36
NG_011526.1:g.24736_24738del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361682.11:c.-1+186_-1+188del MANE Select	ENSP00000354511.6:n.-1+186_-1+188del
ENST00000428707.2:c.-1+186_-1+188del	ENSP00000387695.2:n.-1+186_-1+188del
ENST00000676678.1:c.-1+186_-1+188del	ENSP00000503719.1:n.-1+186_-1+188del
ENST00000678255.1:c.-831+186_-831+188del	ENSP00000504402.1:n.-831+186_-831+188del
ENST00000678769.1:c.-1+186_-1+188del	ENSP00000503289.1:n.-1+186_-1+188del
ENST00000678868.1:c.-1+186_-1+188del	ENSP00000503583.1:n.-1+186_-1+188del
ENST00000207636.9:c.-1+186_-1+188del	ENSP00000207636.5:n.-1+186_-1+188del
ENST00000361682.10:c.-1+186_-1+188del	ENSP00000354511.6:n.-1+186_-1+188del
ENST00000403184.5:c.-1+186_-1+188del	ENSP00000383966.1:n.-1+186_-1+188del
ENST00000403710.5:c.-295+186_-295+188del	ENSP00000385917.1:n.-295+186_-295+188del
ENST00000406520.7:c.-1+186_-1+188del	ENSP00000385150.3:n.-1+186_-1+188del
ENST00000407537.5:c.-179+186_-179+188del	ENSP00000384654.2:n.-179+186_-179+188del
ENST00000412786.5:c.-1+186_-1+188del	ENSP00000403958.1:n.-1+186_-1+188del
ENST00000467943.5:n.196+186_196+188del
NM_000754.3:c.-1+186_-1+188del	NP_000745.1:n.-1+186_-1+188del
NM_001135161.1:c.-1+186_-1+188del	NP_001128633.1:n.-1+186_-1+188del
NM_001135162.1:c.-1+186_-1+188del	NP_001128634.1:n.-1+186_-1+188del
XM_011529885.1:c.114+186_114+188del	XP_011528187.1:n.114+186_114+188del
XM_011529886.1:c.114+186_114+188del	XP_011528188.1:n.114+186_114+188del
XM_011529887.1:c.-1+186_-1+188del	XP_011528189.1:n.-1+186_-1+188del
XM_011529888.1:c.-1+186_-1+188del	XP_011528190.1:n.-1+186_-1+188del
XM_011529889.1:c.-1+186_-1+188del	XP_011528191.1:n.-1+186_-1+188del
XM_011529890.1:c.-295+186_-295+188del	XP_011528192.1:n.-295+186_-295+188del
XM_011529891.1:c.-295+186_-295+188del	XP_011528193.1:n.-295+186_-295+188del
NM_001362828.1:c.-295+186_-295+188del	NP_001349757.1:n.-295+186_-295+188del
XM_011529886.2:c.411+186_411+188del	XP_011528188.2:n.411+186_411+188del
XM_017028595.1:c.-295+186_-295+188del	XP_016884084.1:n.-295+186_-295+188del
NM_000754.4:c.-1+186_-1+188del MANE Select	NP_000745.1:n.-1+186_-1+188del
NM_001135161.2:c.-1+186_-1+188del	NP_001128633.1:n.-1+186_-1+188del
NM_001135162.2:c.-1+186_-1+188del	NP_001128634.1:n.-1+186_-1+188del
NM_001362828.2:c.-295+186_-295+188del	NP_001349757.1:n.-295+186_-295+188del