Canonical Allele Identifier: CA1519939866

Gene: F11 F11-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288579G= , CM000666.2:g.186288579G=	GRCh38
NC_000004.11:g.187209733G= , CM000666.1:g.187209733G=	GRCh37
NC_000004.10:g.187446727G=	NCBI36
NG_008051.1:g.27616G= , LRG_583:g.27616G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1843G= (F11) MANE Select	ENSP00000384957.2:p.Val615=
ENST00000264691.4:c.443G= (F11)
ENST00000264692.8:c.1681G= (F11)	ENSP00000264692.5:p.Val561=
ENST00000403665.6:c.1843G= (F11)	ENSP00000384957.2:p.Val615=
ENST00000503841.1:n.362G= (F11)
NM_000128.3:c.1843G= , LRG_583t1:c.1843G= (F11)	NP_000119.1:p.Val615=
NR_033900.1:n.915C= (F11-AS1)
XM_005262821.2:c.1846G= (F11)	XP_005262878.1:p.Val616=
XM_005262822.2:c.1750G= (F11)	XP_005262879.1:p.Val584=
XM_005262823.2:c.1576G= (F11)	XP_005262880.1:p.Val526=
XM_006714137.1:c.1798G= (F11)	XP_006714200.1:p.Val600=
XM_005262821.4:c.1846G= (F11)	XP_005262878.1:p.Val616=
XM_005262822.4:c.1750G= (F11)	XP_005262879.1:p.Val584=
XM_005262823.4:c.1576G= (F11)	XP_005262880.1:p.Val526=
XM_006714137.3:c.1798G= (F11)	XP_006714200.1:p.Val600=
NM_000128.4:c.1843G= (F11) MANE Select	NP_000119.1:p.Val615=