Canonical Allele Identifier: CA1926617670

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.88990054_88990055delinsTG , CM000672.2:g.88990054_88990055delinsTG GRCh38
NC_000010.10:g.90749811_90749812delinsTG , CM000672.1:g.90749811_90749812delinsTG GRCh37
NC_000010.9:g.90739791_90739792delinsTG NCBI36
NG_009089.2:g.4524_4525delinsTG , LRG_134:g.4524_4525delinsTG
NG_011541.1:g.6336_6337delinsCA , LRG_781:g.6336_6337delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000415557.2:c.-24+884_-24+885delinsCA (ACTA2) ENSP00000396730.2:n.-24+884_-24+885delins...
ENST00000458159.6:c.-24+967_-24+968delinsCA (ACTA2) ENSP00000398239.2:n.-24+967_-24+968delins...
ENST00000696723.1:n.3663+475_3663+476delinsTG (FAS)
ENST00000696992.1:n.1147+475_1147+476delinsTG (FAS)
ENST00000688239.1:n.372-152_372-151delinsTG (FAS)
ENST00000690268.1:c.111+475_111+476delinsTG (FAS) ENSP00000509810.1:n.111+475_111+476delins...
ENST00000415557.1:c.-24+884_-24+885delinsCA (ACTA2) ENSP00000396730.1:n.-24+884_-24+885delins...
ENST00000458159.5:c.-24+967_-24+968delinsCA (ACTA2) ENSP00000398239.1:n.-24+967_-24+968delins...
ENST00000458208.5:c.-24+884_-24+885delinsCA (ACTA2) ENSP00000402373.1:n.-24+884_-24+885delins...
NM_001141945.1:c.-24+884_-24+885delinsCA , LRG_781t2:c.-24+884_-24+885delinsCA (ACTA2) NP_001135417.1:n.-24+884_-24+885delinsCA
XM_006717819.2:c.111+475_111+476delinsTG (FAS) XP_006717882.1:n.111+475_111+476delinsTG
XM_011539764.1:c.192+475_192+476delinsTG (FAS) XP_011538066.1:n.192+475_192+476delinsTG
XM_011539765.1:c.192+475_192+476delinsTG (FAS) XP_011538067.1:n.192+475_192+476delinsTG
XM_011539766.1:c.111+475_111+476delinsTG (FAS) XP_011538068.1:n.111+475_111+476delinsTG
XM_011540016.1:c.-24+967_-24+968delinsCA (ACTA2) XP_011538318.1:n.-24+967_-24+968delinsCA
XR_945732.1:n.207+475_207+476delinsTG (FAS)
XR_945733.1:n.207+475_207+476delinsTG (FAS)
NM_001141945.2:c.-24+884_-24+885delinsCA (ACTA2) NP_001135417.1:n.-24+884_-24+885delinsCA
NM_001320855.1:c.-24+967_-24+968delinsCA (ACTA2) NP_001307784.1:n.-24+967_-24+968delinsCA
XM_006717819.3:c.111+475_111+476delinsTG (FAS) XP_006717882.1:n.111+475_111+476delinsTG
XM_011539764.2:c.192+475_192+476delinsTG (FAS) XP_011538066.1:n.192+475_192+476delinsTG
XM_011539765.2:c.192+475_192+476delinsTG (FAS) XP_011538067.1:n.192+475_192+476delinsTG
XM_011539766.2:c.111+475_111+476delinsTG (FAS) XP_011538068.1:n.111+475_111+476delinsTG
XR_945732.3:n.207+475_207+476delinsTG (FAS)
XR_945733.2:n.207+475_207+476delinsTG (FAS)