Canonical Allele Identifier: CA2764876922

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186288704_186288705insAACACACC , CM000666.2:g.186288704_186288705insAACACACC GRCh38
NC_000004.11:g.187209858_187209859insAACACACC , CM000666.1:g.187209858_187209859insAACACACC GRCh37
NC_000004.10:g.187446852_187446853insAACACACC NCBI36
NG_008051.1:g.27741_27742insAACACACC , LRG_583:g.27741_27742insAACACACC

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.*90_*91insAACACACC (F11) MANE Select ENSP00000384957.2:n.*90_*91insAACACACC
ENST00000264691.4:c.568_569insAACACACC (F11)
ENST00000264692.8:c.*90_*91insAACACACC (F11) ENSP00000264692.5:n.*90_*91insAACACACC
ENST00000403665.6:c.*90_*91insAACACACC (F11) ENSP00000384957.2:n.*90_*91insAACACACC
ENST00000503841.1:n.487_488insAACACACC (F11)
NM_000128.3:c.*90_*91insAACACACC , LRG_583t1:c.*90_*91insAACACACC (F11) NP_000119.1:n.*90_*91insAACACACC
NR_033900.1:n.789_790insGGTGTGTT (F11-AS1)
XM_005262821.2:c.*90_*91insAACACACC (F11) XP_005262878.1:n.*90_*91insAACACACC
XM_005262822.2:c.*90_*91insAACACACC (F11) XP_005262879.1:n.*90_*91insAACACACC
XM_005262823.2:c.*90_*91insAACACACC (F11) XP_005262880.1:n.*90_*91insAACACACC
XM_006714137.1:c.*90_*91insAACACACC (F11) XP_006714200.1:n.*90_*91insAACACACC
XM_005262821.4:c.*90_*91insAACACACC (F11) XP_005262878.1:n.*90_*91insAACACACC
XM_005262822.4:c.*90_*91insAACACACC (F11) XP_005262879.1:n.*90_*91insAACACACC
XM_005262823.4:c.*90_*91insAACACACC (F11) XP_005262880.1:n.*90_*91insAACACACC
XM_006714137.3:c.*90_*91insAACACACC (F11) XP_006714200.1:n.*90_*91insAACACACC
NM_000128.4:c.*90_*91insAACACACC (F11) MANE Select NP_000119.1:n.*90_*91insAACACACC