Canonical Allele Identifier: CA1519938894

Gene: F11 F11-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186286611T= , CM000666.2:g.186286611T=	GRCh38
NC_000004.11:g.187207765T= , CM000666.1:g.187207765T=	GRCh37
NC_000004.10:g.187444759T=	NCBI36
NG_008051.1:g.25648T= , LRG_583:g.25648T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1576+101T= (F11) MANE Select	ENSP00000384957.2:n.1576+101T=
ENST00000264691.4:c.176+798T= (F11)
ENST00000264692.8:c.1414+101T= (F11)	ENSP00000264692.5:n.1414+101T=
ENST00000403665.6:c.1576+101T= (F11)	ENSP00000384957.2:n.1576+101T=
NM_000128.3:c.1576+101T= , LRG_583t1:c.1576+101T= (F11)	NP_000119.1:n.1576+101T=
NR_033900.1:n.1067-345A= (F11-AS1)
XM_005262821.2:c.1579+101T= (F11)	XP_005262878.1:n.1579+101T=
XM_005262822.2:c.1483+798T= (F11)	XP_005262879.1:n.1483+798T=
XM_005262823.2:c.1309+101T= (F11)	XP_005262880.1:n.1309+101T=
XM_005262824.1:c.1549T= (F11)	XP_005262881.1:p.Tyr517=
XM_006714137.1:c.1531+101T= (F11)	XP_006714200.1:n.1531+101T=
XR_938706.1:n.1984+101T= (F11)
XR_938707.1:n.1888+798T= (F11)
XM_005262821.4:c.1579+101T= (F11)	XP_005262878.1:n.1579+101T=
XM_005262822.4:c.1483+798T= (F11)	XP_005262879.1:n.1483+798T=
XM_005262823.4:c.1309+101T= (F11)	XP_005262880.1:n.1309+101T=
XM_006714137.3:c.1531+101T= (F11)	XP_006714200.1:n.1531+101T=
NM_000128.4:c.1576+101T= (F11) MANE Select	NP_000119.1:n.1576+101T=