Canonical Allele Identifier: CA1519939502

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186287896_186287909delinsTTTTGTTTTTTTTG , CM000666.2:g.186287896_186287909delinsTTTTGTTTTTTTTG GRCh38
NC_000004.11:g.187209050_187209063delinsTTTTGTTTTTTTTG , CM000666.1:g.187209050_187209063delinsTTTTGTTTTTTTTG GRCh37
NC_000004.10:g.187446044_187446057delinsTTTTGTTTTTTTTG NCBI36
NG_008051.1:g.26933_26946delinsTTTTGTTTTTTTTG , LRG_583:g.26933_26946delinsTTTTGTTTTTTTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.1716+73_1716+86delinsTTTTGTTTTTTTTG (F11) MANE Select ENSP00000384957.2:n.1716+73_1716+86delinsTTTTGTTTTTTTTG
ENST00000264691.4:c.316+73_316+86delinsTTTTGTTTTTTTTG (F11)
ENST00000264692.8:c.1554+73_1554+86delinsTTTTGTTTTTTTTG (F11) ENSP00000264692.5:n.1554+73_1554+86delinsTTTTGTTTTTTTTG
ENST00000403665.6:c.1716+73_1716+86delinsTTTTGTTTTTTTTG (F11) ENSP00000384957.2:n.1716+73_1716+86delinsTTTTGTTTTTTTTG
ENST00000503841.1:n.235+73_235+86delinsTTTTGTTTTTTTTG (F11)
NM_000128.3:c.1716+73_1716+86delinsTTTTGTTTTTTTTG , LRG_583t1:c.1716+73_1716+86delinsTTTTGTTTTTTTTG (F11) NP_000119.1:n.1716+73_1716+86delinsTTTTGTTTTTTTTG
NR_033900.1:n.1066+519_1066+532delinsCAAAAAAAACAAAA (F11-AS1)
XM_005262821.2:c.1719+73_1719+86delinsTTTTGTTTTTTTTG (F11) XP_005262878.1:n.1719+73_1719+86delinsTTTTGTTTTTTTTG
XM_005262822.2:c.1623+73_1623+86delinsTTTTGTTTTTTTTG (F11) XP_005262879.1:n.1623+73_1623+86delinsTTTTGTTTTTTTTG
XM_005262823.2:c.1449+73_1449+86delinsTTTTGTTTTTTTTG (F11) XP_005262880.1:n.1449+73_1449+86delinsTTTTGTTTTTTTTG
XM_006714137.1:c.1671+73_1671+86delinsTTTTGTTTTTTTTG (F11) XP_006714200.1:n.1671+73_1671+86delinsTTTTGTTTTTTTTG
XM_005262821.4:c.1719+73_1719+86delinsTTTTGTTTTTTTTG (F11) XP_005262878.1:n.1719+73_1719+86delinsTTTTGTTTTTTTTG
XM_005262822.4:c.1623+73_1623+86delinsTTTTGTTTTTTTTG (F11) XP_005262879.1:n.1623+73_1623+86delinsTTTTGTTTTTTTTG
XM_005262823.4:c.1449+73_1449+86delinsTTTTGTTTTTTTTG (F11) XP_005262880.1:n.1449+73_1449+86delinsTTTTGTTTTTTTTG
XM_006714137.3:c.1671+73_1671+86delinsTTTTGTTTTTTTTG (F11) XP_006714200.1:n.1671+73_1671+86delinsTTTTGTTTTTTTTG
NM_000128.4:c.1716+73_1716+86delinsTTTTGTTTTTTTTG (F11) MANE Select NP_000119.1:n.1716+73_1716+86delinsTTTTGTTTTTTTTG