Canonical Allele Identifier: CA1519939748

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186288335G= , CM000666.2:g.186288335G= GRCh38
NC_000004.11:g.187209489G= , CM000666.1:g.187209489G= GRCh37
NC_000004.10:g.187446483G= NCBI36
NG_008051.1:g.27372G= , LRG_583:g.27372G=

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1717-118G= (F11) MANE Select ENSP00000384957.2:n.1717-118G=
ENST00000264691.4:c.317-118G= (F11)
ENST00000264692.8:c.1555-118G= (F11) ENSP00000264692.5:n.1555-118G=
ENST00000403665.6:c.1717-118G= (F11) ENSP00000384957.2:n.1717-118G=
ENST00000503841.1:n.236-118G= (F11)
NM_000128.3:c.1717-118G= , LRG_583t1:c.1717-118G= (F11) NP_000119.1:n.1717-118G=
NR_033900.1:n.1066+93C= (F11-AS1)
XM_005262821.2:c.1720-118G= (F11) XP_005262878.1:n.1720-118G=
XM_005262822.2:c.1624-118G= (F11) XP_005262879.1:n.1624-118G=
XM_005262823.2:c.1450-118G= (F11) XP_005262880.1:n.1450-118G=
XM_006714137.1:c.1672-118G= (F11) XP_006714200.1:n.1672-118G=
XM_005262821.4:c.1720-118G= (F11) XP_005262878.1:n.1720-118G=
XM_005262822.4:c.1624-118G= (F11) XP_005262879.1:n.1624-118G=
XM_005262823.4:c.1450-118G= (F11) XP_005262880.1:n.1450-118G=
XM_006714137.3:c.1672-118G= (F11) XP_006714200.1:n.1672-118G=
NM_000128.4:c.1717-118G= (F11) MANE Select NP_000119.1:n.1717-118G=