Canonical Allele Identifier: CA1519939818

Gene: F11 F11-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288492G= , CM000666.2:g.186288492G=	GRCh38
NC_000004.11:g.187209646G= , CM000666.1:g.187209646G=	GRCh37
NC_000004.10:g.187446640G=	NCBI36
NG_008051.1:g.27529G= , LRG_583:g.27529G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1756G= (F11) MANE Select	ENSP00000384957.2:p.Val586=
ENST00000264691.4:c.356G= (F11)
ENST00000264692.8:c.1594G= (F11)	ENSP00000264692.5:p.Val532=
ENST00000403665.6:c.1756G= (F11)	ENSP00000384957.2:p.Val586=
ENST00000503841.1:n.275G= (F11)
NM_000128.3:c.1756G= , LRG_583t1:c.1756G= (F11)	NP_000119.1:p.Val586=
NR_033900.1:n.1002C= (F11-AS1)
XM_005262821.2:c.1759G= (F11)	XP_005262878.1:p.Val587=
XM_005262822.2:c.1663G= (F11)	XP_005262879.1:p.Val555=
XM_005262823.2:c.1489G= (F11)	XP_005262880.1:p.Val497=
XM_006714137.1:c.1711G= (F11)	XP_006714200.1:p.Val571=
XM_005262821.4:c.1759G= (F11)	XP_005262878.1:p.Val587=
XM_005262822.4:c.1663G= (F11)	XP_005262879.1:p.Val555=
XM_005262823.4:c.1489G= (F11)	XP_005262880.1:p.Val497=
XM_006714137.3:c.1711G= (F11)	XP_006714200.1:p.Val571=
NM_000128.4:c.1756G= (F11) MANE Select	NP_000119.1:p.Val586=