Canonical Allele Identifier: CA1519939415

Gene: F11 F11-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287726T= , CM000666.2:g.186287726T=	GRCh38
NC_000004.11:g.187208880T= , CM000666.1:g.187208880T=	GRCh37
NC_000004.10:g.187445874T=	NCBI36
NG_008051.1:g.26763T= , LRG_583:g.26763T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1619T= (F11) MANE Select	ENSP00000384957.2:p.Val540=
ENST00000264691.4:c.219T= (F11)
ENST00000264692.8:c.1457T= (F11)	ENSP00000264692.5:p.Val486=
ENST00000403665.6:c.1619T= (F11)	ENSP00000384957.2:p.Val540=
ENST00000503841.1:n.138T= (F11)
NM_000128.3:c.1619T= , LRG_583t1:c.1619T= (F11)	NP_000119.1:p.Val540=
NR_033900.1:n.1066+702A= (F11-AS1)
XM_005262821.2:c.1622T= (F11)	XP_005262878.1:p.Val541=
XM_005262822.2:c.1526T= (F11)	XP_005262879.1:p.Val509=
XM_005262823.2:c.1352T= (F11)	XP_005262880.1:p.Val451=
XM_006714137.1:c.1574T= (F11)	XP_006714200.1:p.Val525=
XR_938707.1:n.1931T= (F11)
XM_005262821.4:c.1622T= (F11)	XP_005262878.1:p.Val541=
XM_005262822.4:c.1526T= (F11)	XP_005262879.1:p.Val509=
XM_005262823.4:c.1352T= (F11)	XP_005262880.1:p.Val451=
XM_006714137.3:c.1574T= (F11)	XP_006714200.1:p.Val525=
NM_000128.4:c.1619T= (F11) MANE Select	NP_000119.1:p.Val540=