Canonical Allele Identifier: CA1519938820

Gene: F11 F11-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186286460T= , CM000666.2:g.186286460T=	GRCh38
NC_000004.11:g.187207614T= , CM000666.1:g.187207614T=	GRCh37
NC_000004.10:g.187444608T=	NCBI36
NG_008051.1:g.25497T= , LRG_583:g.25497T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1526T= (F11) MANE Select	ENSP00000384957.2:p.Val509=
ENST00000264691.4:c.176+647T= (F11)
ENST00000264692.8:c.1364T= (F11)	ENSP00000264692.5:p.Val455=
ENST00000403665.6:c.1526T= (F11)	ENSP00000384957.2:p.Val509=
NM_000128.3:c.1526T= , LRG_583t1:c.1526T= (F11)	NP_000119.1:p.Val509=
NR_033900.1:n.1067-194A= (F11-AS1)
XM_005262821.2:c.1529T= (F11)	XP_005262878.1:p.Val510=
XM_005262822.2:c.1483+647T= (F11)	XP_005262879.1:n.1483+647T=
XM_005262823.2:c.1259T= (F11)	XP_005262880.1:p.Val420=
XM_005262824.1:c.1484-86T= (F11)	XP_005262881.1:n.1484-86T=
XM_006714137.1:c.1481T= (F11)	XP_006714200.1:p.Val494=
XR_938706.1:n.1934T= (F11)
XR_938707.1:n.1888+647T= (F11)
XM_005262821.4:c.1529T= (F11)	XP_005262878.1:p.Val510=
XM_005262822.4:c.1483+647T= (F11)	XP_005262879.1:n.1483+647T=
XM_005262823.4:c.1259T= (F11)	XP_005262880.1:p.Val420=
XM_006714137.3:c.1481T= (F11)	XP_006714200.1:p.Val494=
XR_001741172.2:n.2000T= (F11)
NM_000128.4:c.1526T= (F11) MANE Select	NP_000119.1:p.Val509=