Canonical Allele Identifier: CA1139781690

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19968911_19968916delinsTTTTTT , CM000684.2:g.19968911_19968916delinsTTTTTT GRCh38
NC_000022.10:g.19956434_19956439delinsTTTTTT , CM000684.1:g.19956434_19956439delinsTTTTTT GRCh37
NC_000022.9:g.18336434_18336439delinsTTTTTT NCBI36
NG_011526.1:g.32172_32177delinsTTTTTT
NG_023326.1:g.52871_52876delinsAAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000361682.11:c.*175_*180delinsTTTTTT (COMT) MANE Select ENSP00000354511.6:n.*175_*180delinsTTTTTT
ENST00000428707.2:c.*1484_*1489delinsTTTTTT (COMT) ENSP00000387695.2:n.*1484_*1489delinsTTTTTT
ENST00000676678.1:c.*175_*180delinsTTTTTT (COMT) ENSP00000503719.1:n.*175_*180delinsTTTTTT
ENST00000677397.1:c.*570_*575delinsTTTTTT (COMT) ENSP00000503422.1:n.*570_*575delinsTTTTTT
ENST00000677470.1:n.841_846delinsTTTTTT (COMT)
ENST00000677564.1:n.774_779delinsTTTTTT (COMT)
ENST00000677675.1:n.791_796delinsTTTTTT (COMT)
ENST00000678255.1:c.*175_*180delinsTTTTTT (COMT) ENSP00000504402.1:n.*175_*180delinsTTTTTT
ENST00000678769.1:c.*175_*180delinsTTTTTT (COMT) ENSP00000503289.1:n.*175_*180delinsTTTTTT
ENST00000678868.1:c.*175_*180delinsTTTTTT (COMT) ENSP00000503583.1:n.*175_*180delinsTTTTTT
ENST00000678945.1:n.859_864delinsTTTTTT (COMT)
ENST00000207636.9:c.*449_*454delinsTTTTTT (COMT) ENSP00000207636.5:n.*449_*454delinsTTTTTT
ENST00000361682.10:c.*175_*180delinsTTTTTT (COMT) ENSP00000354511.6:n.*175_*180delinsTTTTTT
ENST00000403710.5:c.*175_*180delinsTTTTTT (COMT) ENSP00000385917.1:n.*175_*180delinsTTTTTT
ENST00000406520.7:c.*175_*180delinsTTTTTT (COMT) ENSP00000385150.3:n.*175_*180delinsTTTTTT
ENST00000407537.5:c.*175_*180delinsTTTTTT (COMT) ENSP00000384654.2:n.*175_*180delinsTTTTTT
ENST00000449653.5:c.*175_*180delinsTTTTTT (COMT) ENSP00000416778.1:n.*175_*180delinsTTTTTT
NM_000754.3:c.*175_*180delinsTTTTTT (COMT) NP_000745.1:n.*175_*180delinsTTTTTT
NM_001135161.1:c.*175_*180delinsTTTTTT (COMT) NP_001128633.1:n.*175_*180delinsTTTTTT
NM_001135162.1:c.*175_*180delinsTTTTTT (COMT) NP_001128634.1:n.*175_*180delinsTTTTTT
NM_007310.2:c.*175_*180delinsTTTTTT (COMT) NP_009294.1:n.*175_*180delinsTTTTTT
XM_005261242.1:c.2764-1707_2764-1702delinsAAAAAA (ARVCF) XP_005261299.1:n.2764-1707_2764-1702delinsAAAAAA
XM_006724243.1:c.2782-1707_2782-1702delinsAAAAAA (ARVCF) XP_006724306.1:n.2782-1707_2782-1702delinsAAAAAA
XM_006724246.2:c.2536-1707_2536-1702delinsAAAAAA (ARVCF) XP_006724309.1:n.2536-1707_2536-1702delinsAAAAAA
XM_011529886.1:c.*175_*180delinsTTTTTT (COMT) XP_011528188.1:n.*175_*180delinsTTTTTT
XM_011530179.1:c.2749-1707_2749-1702delinsAAAAAA (ARVCF) XP_011528481.1:n.2749-1707_2749-1702delinsAAAAAA
XM_011530182.1:c.1348-1707_1348-1702delinsAAAAAA (ARVCF) XP_011528484.1:n.1348-1707_1348-1702delinsAAAAAA
NM_001362828.1:c.*175_*180delinsTTTTTT (COMT) NP_001349757.1:n.*175_*180delinsTTTTTT
XM_005261242.3:c.2764-1707_2764-1702delinsAAAAAA (ARVCF) XP_005261299.1:n.2764-1707_2764-1702delinsAAAAAA
XM_006724243.3:c.2782-1707_2782-1702delinsAAAAAA (ARVCF) XP_006724306.1:n.2782-1707_2782-1702delinsAAAAAA
XM_006724246.4:c.2536-1707_2536-1702delinsAAAAAA (ARVCF) XP_006724309.1:n.2536-1707_2536-1702delinsAAAAAA
XM_011529886.2:c.*175_*180delinsTTTTTT (COMT) XP_011528188.2:n.*175_*180delinsTTTTTT
XM_011530179.3:c.2749-1707_2749-1702delinsAAAAAA (ARVCF) XP_011528481.1:n.2749-1707_2749-1702delinsAAAAAA
XM_011530182.3:c.1348-1707_1348-1702delinsAAAAAA (ARVCF) XP_011528484.1:n.1348-1707_1348-1702delinsAAAAAA
XM_017028595.1:c.*175_*180delinsTTTTTT (COMT) XP_016884084.1:n.*175_*180delinsTTTTTT
XM_024452249.1:c.2536-1707_2536-1702delinsAAAAAA (ARVCF) XP_024308017.1:n.2536-1707_2536-1702delinsAAAAAA
NM_000754.4:c.*175_*180delinsTTTTTT (COMT) MANE Select NP_000745.1:n.*175_*180delinsTTTTTT
NM_001135161.2:c.*175_*180delinsTTTTTT (COMT) NP_001128633.1:n.*175_*180delinsTTTTTT
NM_001135162.2:c.*175_*180delinsTTTTTT (COMT) NP_001128634.1:n.*175_*180delinsTTTTTT
NM_001362828.2:c.*175_*180delinsTTTTTT (COMT) NP_001349757.1:n.*175_*180delinsTTTTTT
NM_007310.3:c.*175_*180delinsTTTTTT (COMT) NP_009294.1:n.*175_*180delinsTTTTTT