Canonical Allele Identifier: CA1519939878

Gene: F11 F11-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288611G= , CM000666.2:g.186288611G=	GRCh38
NC_000004.11:g.187209765G= , CM000666.1:g.187209765G=	GRCh37
NC_000004.10:g.187446759G=	NCBI36
NG_008051.1:g.27648G= , LRG_583:g.27648G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1875G= (F11) MANE Select	ENSP00000384957.2:p.Val625=
ENST00000264691.4:c.475G= (F11)
ENST00000264692.8:c.1713G= (F11)	ENSP00000264692.5:p.Val571=
ENST00000403665.6:c.1875G= (F11)	ENSP00000384957.2:p.Val625=
ENST00000503841.1:n.394G= (F11)
NM_000128.3:c.1875G= , LRG_583t1:c.1875G= (F11)	NP_000119.1:p.Val625=
NR_033900.1:n.883C= (F11-AS1)
XM_005262821.2:c.1878G= (F11)	XP_005262878.1:p.Val626=
XM_005262822.2:c.1782G= (F11)	XP_005262879.1:p.Val594=
XM_005262823.2:c.1608G= (F11)	XP_005262880.1:p.Val536=
XM_006714137.1:c.1830G= (F11)	XP_006714200.1:p.Val610=
XM_005262821.4:c.1878G= (F11)	XP_005262878.1:p.Val626=
XM_005262822.4:c.1782G= (F11)	XP_005262879.1:p.Val594=
XM_005262823.4:c.1608G= (F11)	XP_005262880.1:p.Val536=
XM_006714137.3:c.1830G= (F11)	XP_006714200.1:p.Val610=
NM_000128.4:c.1875G= (F11) MANE Select	NP_000119.1:p.Val625=