Canonical Allele Identifier: CA1519939414

Gene: F11 F11-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287725G= , CM000666.2:g.186287725G=	GRCh38
NC_000004.11:g.187208879G= , CM000666.1:g.187208879G=	GRCh37
NC_000004.10:g.187445873G=	NCBI36
NG_008051.1:g.26762G= , LRG_583:g.26762G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1618G= (F11) MANE Select	ENSP00000384957.2:p.Val540=
ENST00000264691.4:c.218G= (F11)
ENST00000264692.8:c.1456G= (F11)	ENSP00000264692.5:p.Val486=
ENST00000403665.6:c.1618G= (F11)	ENSP00000384957.2:p.Val540=
ENST00000503841.1:n.137G= (F11)
NM_000128.3:c.1618G= , LRG_583t1:c.1618G= (F11)	NP_000119.1:p.Val540=
NR_033900.1:n.1066+703C= (F11-AS1)
XM_005262821.2:c.1621G= (F11)	XP_005262878.1:p.Val541=
XM_005262822.2:c.1525G= (F11)	XP_005262879.1:p.Val509=
XM_005262823.2:c.1351G= (F11)	XP_005262880.1:p.Val451=
XM_006714137.1:c.1573G= (F11)	XP_006714200.1:p.Val525=
XR_938707.1:n.1930G= (F11)
XM_005262821.4:c.1621G= (F11)	XP_005262878.1:p.Val541=
XM_005262822.4:c.1525G= (F11)	XP_005262879.1:p.Val509=
XM_005262823.4:c.1351G= (F11)	XP_005262880.1:p.Val451=
XM_006714137.3:c.1573G= (F11)	XP_006714200.1:p.Val525=
NM_000128.4:c.1618G= (F11) MANE Select	NP_000119.1:p.Val540=