Canonical Allele Identifier: CA1519939880

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186288615A= , CM000666.2:g.186288615A= GRCh38
NC_000004.11:g.187209769A= , CM000666.1:g.187209769A= GRCh37
NC_000004.10:g.187446763A= NCBI36
NG_008051.1:g.27652A= , LRG_583:g.27652A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.*1A= (F11) MANE Select ENSP00000384957.2:n.*1A=
ENST00000264691.4:c.479A= (F11)
ENST00000264692.8:c.*1A= (F11) ENSP00000264692.5:n.*1A=
ENST00000403665.6:c.*1A= (F11) ENSP00000384957.2:n.*1A=
ENST00000503841.1:n.398A= (F11)
NM_000128.3:c.*1A= , LRG_583t1:c.*1A= (F11) NP_000119.1:n.*1A=
NR_033900.1:n.879T= (F11-AS1)
XM_005262821.2:c.*1A= (F11) XP_005262878.1:n.*1A=
XM_005262822.2:c.*1A= (F11) XP_005262879.1:n.*1A=
XM_005262823.2:c.*1A= (F11) XP_005262880.1:n.*1A=
XM_006714137.1:c.*1A= (F11) XP_006714200.1:n.*1A=
XM_005262821.4:c.*1A= (F11) XP_005262878.1:n.*1A=
XM_005262822.4:c.*1A= (F11) XP_005262879.1:n.*1A=
XM_005262823.4:c.*1A= (F11) XP_005262880.1:n.*1A=
XM_006714137.3:c.*1A= (F11) XP_006714200.1:n.*1A=
NM_000128.4:c.*1A= (F11) MANE Select NP_000119.1:n.*1A=