Canonical Allele Identifier: CA10104452
Gene: COMT HGNC NCBI

Linked Data

dbSNP Id: rs755100597

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19962581_19962582dup , CM000684.2:g.19962581_19962582dup GRCh38
NC_000022.10:g.19950104_19950105dup , CM000684.1:g.19950104_19950105dup GRCh37
NC_000022.9:g.18330104_18330105dup NCBI36
NG_011526.1:g.25842_25843dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000361682.11:c.55_56dup MANE Select ENSP00000354511.6:p.Val20TrpfsTer8
ENST00000428707.2:c.55_56dup ENSP00000387695.2:p.Val20TrpfsTer8
ENST00000676678.1:c.55_56dup ENSP00000503719.1:p.Val20TrpfsTer8
ENST00000678255.1:c.55_56dup ENSP00000504402.1:p.Val20TrpfsTer8
ENST00000678769.1:c.55_56dup ENSP00000503289.1:p.Val20TrpfsTer8
ENST00000678868.1:c.55_56dup ENSP00000503583.1:p.Val20TrpfsTer8
ENST00000207636.9:c.55_56dup ENSP00000207636.5:p.Val20TrpfsTer8
ENST00000361682.10:c.55_56dup ENSP00000354511.6:p.Val20TrpfsTer8
ENST00000403184.5:c.55_56dup ENSP00000383966.1:p.Val20TrpfsTer8
ENST00000403710.5:c.55_56dup ENSP00000385917.1:p.Val20TrpfsTer8
ENST00000406520.7:c.55_56dup ENSP00000385150.3:p.Val20TrpfsTer8
ENST00000407537.5:c.55_56dup ENSP00000384654.2:p.Val20TrpfsTer8
ENST00000412786.5:c.55_56dup ENSP00000403958.1:p.Val20TrpfsTer8
ENST00000449653.5:c.-96_-95dup ENSP00000416778.1:n.-96_-95dup
ENST00000467943.5:n.251_252dup
NM_000754.3:c.55_56dup NP_000745.1:p.Val20TrpfsTer8
NM_001135161.1:c.55_56dup NP_001128633.1:p.Val20TrpfsTer8
NM_001135162.1:c.55_56dup NP_001128634.1:p.Val20TrpfsTer8
NM_007310.2:c.-96_-95dup NP_009294.1:n.-96_-95dup
XM_011529885.1:c.169_170dup XP_011528187.1:p.Val58TrpfsTer8
XM_011529886.1:c.169_170dup XP_011528188.1:p.Val58TrpfsTer8
XM_011529887.1:c.55_56dup XP_011528189.1:p.Val20TrpfsTer8
XM_011529888.1:c.55_56dup XP_011528190.1:p.Val20TrpfsTer8
XM_011529889.1:c.55_56dup XP_011528191.1:p.Val20TrpfsTer8
XM_011529890.1:c.55_56dup XP_011528192.1:p.Val20TrpfsTer8
XM_011529891.1:c.55_56dup XP_011528193.1:p.Val20TrpfsTer8
NM_001362828.1:c.55_56dup NP_001349757.1:p.Val20TrpfsTer8
XM_011529886.2:c.466_467dup XP_011528188.2:p.Val157TrpfsTer8
XM_017028595.1:c.55_56dup XP_016884084.1:p.Val20TrpfsTer8
NM_000754.4:c.55_56dup MANE Select NP_000745.1:p.Val20TrpfsTer8
NM_001135161.2:c.55_56dup NP_001128633.1:p.Val20TrpfsTer8
NM_001135162.2:c.55_56dup NP_001128634.1:p.Val20TrpfsTer8
NM_001362828.2:c.55_56dup NP_001349757.1:p.Val20TrpfsTer8
NM_007310.3:c.-96_-95dup NP_009294.1:n.-96_-95dup