Canonical Allele Identifier: CA2655332030

Gene: COMT

Linked Data

• gnomAD v4: 22-19962336-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19962336G>T , CM000684.2:g.19962336G>T	GRCh38
NC_000022.10:g.19949859G>T , CM000684.1:g.19949859G>T	GRCh37
NC_000022.9:g.18329859G>T	NCBI36
NG_011526.1:g.25597G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000361682.11:c.1-191G>T MANE Select	ENSP00000354511.6:n.1-191G>T
ENST00000428707.2:c.1-191G>T	ENSP00000387695.2:n.1-191G>T
ENST00000676678.1:c.1-191G>T	ENSP00000503719.1:n.1-191G>T
ENST00000678255.1:c.-191G>T	ENSP00000504402.1:n.-191G>T
ENST00000678769.1:c.1-191G>T	ENSP00000503289.1:n.1-191G>T
ENST00000678868.1:c.1-191G>T	ENSP00000503583.1:n.1-191G>T
ENST00000207636.9:c.1-191G>T	ENSP00000207636.5:n.1-191G>T
ENST00000361682.10:c.1-191G>T	ENSP00000354511.6:n.1-191G>T
ENST00000403184.5:c.1-191G>T	ENSP00000383966.1:n.1-191G>T
ENST00000403710.5:c.-191G>T	ENSP00000385917.1:n.-191G>T
ENST00000406520.7:c.1-191G>T	ENSP00000385150.3:n.1-191G>T
ENST00000407537.5:c.1-191G>T	ENSP00000384654.2:n.1-191G>T
ENST00000412786.5:c.1-191G>T	ENSP00000403958.1:n.1-191G>T
ENST00000467943.5:n.197-191G>T
NM_000754.3:c.1-191G>T	NP_000745.1:n.1-191G>T
NM_001135161.1:c.1-191G>T	NP_001128633.1:n.1-191G>T
NM_001135162.1:c.1-191G>T	NP_001128634.1:n.1-191G>T
XM_011529885.1:c.115-191G>T	XP_011528187.1:n.115-191G>T
XM_011529886.1:c.115-191G>T	XP_011528188.1:n.115-191G>T
XM_011529887.1:c.1-191G>T	XP_011528189.1:n.1-191G>T
XM_011529888.1:c.1-191G>T	XP_011528190.1:n.1-191G>T
XM_011529889.1:c.1-191G>T	XP_011528191.1:n.1-191G>T
XM_011529890.1:c.-191G>T	XP_011528192.1:n.-191G>T
XM_011529891.1:c.-191G>T	XP_011528193.1:n.-191G>T
NM_001362828.1:c.-191G>T	NP_001349757.1:n.-191G>T
XM_011529886.2:c.412-191G>T	XP_011528188.2:n.412-191G>T
XM_017028595.1:c.-191G>T	XP_016884084.1:n.-191G>T
NM_000754.4:c.1-191G>T MANE Select	NP_000745.1:n.1-191G>T
NM_001135161.2:c.1-191G>T	NP_001128633.1:n.1-191G>T
NM_001135162.2:c.1-191G>T	NP_001128634.1:n.1-191G>T
NM_001362828.2:c.-191G>T	NP_001349757.1:n.-191G>T