Canonical Allele Identifier: CA2655336625

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19969192G>T , CM000684.2:g.19969192G>T GRCh38
NC_000022.10:g.19956715G>T , CM000684.1:g.19956715G>T GRCh37
NC_000022.9:g.18336715G>T NCBI36
NG_011526.1:g.32453G>T
NG_023326.1:g.52595C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361682.11:c.*456G>T (COMT) MANE Select ENSP00000354511.6:n.*456G>T
ENST00000677564.1:n.1055G>T (COMT)
ENST00000678255.1:c.*456G>T (COMT) ENSP00000504402.1:n.*456G>T
ENST00000678769.1:c.*456G>T (COMT) ENSP00000503289.1:n.*456G>T
ENST00000678868.1:c.*456G>T (COMT) ENSP00000503583.1:n.*456G>T
ENST00000678945.1:n.1140G>T (COMT)
ENST00000361682.10:c.*456G>T (COMT) ENSP00000354511.6:n.*456G>T
NM_000754.3:c.*456G>T (COMT) NP_000745.1:n.*456G>T
NM_001135161.1:c.*456G>T (COMT) NP_001128633.1:n.*456G>T
NM_001135162.1:c.*456G>T (COMT) NP_001128634.1:n.*456G>T
NM_007310.2:c.*456G>T (COMT) NP_009294.1:n.*456G>T
XM_005261242.1:c.2764-1983C>A (ARVCF) XP_005261299.1:n.2764-1983C>A
XM_006724243.1:c.2782-1983C>A (ARVCF) XP_006724306.1:n.2782-1983C>A
XM_006724246.2:c.2536-1983C>A (ARVCF) XP_006724309.1:n.2536-1983C>A
XM_011530179.1:c.2749-1983C>A (ARVCF) XP_011528481.1:n.2749-1983C>A
XM_011530182.1:c.1348-1983C>A (ARVCF) XP_011528484.1:n.1348-1983C>A
NM_001362828.1:c.*456G>T (COMT) NP_001349757.1:n.*456G>T
XM_005261242.3:c.2764-1983C>A (ARVCF) XP_005261299.1:n.2764-1983C>A
XM_006724243.3:c.2782-1983C>A (ARVCF) XP_006724306.1:n.2782-1983C>A
XM_006724246.4:c.2536-1983C>A (ARVCF) XP_006724309.1:n.2536-1983C>A
XM_011530179.3:c.2749-1983C>A (ARVCF) XP_011528481.1:n.2749-1983C>A
XM_011530182.3:c.1348-1983C>A (ARVCF) XP_011528484.1:n.1348-1983C>A
XM_024452249.1:c.2536-1983C>A (ARVCF) XP_024308017.1:n.2536-1983C>A
NM_000754.4:c.*456G>T (COMT) MANE Select NP_000745.1:n.*456G>T
NM_001135161.2:c.*456G>T (COMT) NP_001128633.1:n.*456G>T
NM_001135162.2:c.*456G>T (COMT) NP_001128634.1:n.*456G>T
NM_001362828.2:c.*456G>T (COMT) NP_001349757.1:n.*456G>T
NM_007310.3:c.*456G>T (COMT) NP_009294.1:n.*456G>T