Canonical Allele Identifier: CA1519939841

Gene: F11 F11-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288534G= , CM000666.2:g.186288534G=	GRCh38
NC_000004.11:g.187209688G= , CM000666.1:g.187209688G=	GRCh37
NC_000004.10:g.187446682G=	NCBI36
NG_008051.1:g.27571G= , LRG_583:g.27571G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1798G= (F11) MANE Select	ENSP00000384957.2:p.Ala600=
ENST00000264691.4:c.398G= (F11)
ENST00000264692.8:c.1636G= (F11)	ENSP00000264692.5:p.Ala546=
ENST00000403665.6:c.1798G= (F11)	ENSP00000384957.2:p.Ala600=
ENST00000503841.1:n.317G= (F11)
NM_000128.3:c.1798G= , LRG_583t1:c.1798G= (F11)	NP_000119.1:p.Ala600=
NR_033900.1:n.960C= (F11-AS1)
XM_005262821.2:c.1801G= (F11)	XP_005262878.1:p.Ala601=
XM_005262822.2:c.1705G= (F11)	XP_005262879.1:p.Ala569=
XM_005262823.2:c.1531G= (F11)	XP_005262880.1:p.Ala511=
XM_006714137.1:c.1753G= (F11)	XP_006714200.1:p.Ala585=
XM_005262821.4:c.1801G= (F11)	XP_005262878.1:p.Ala601=
XM_005262822.4:c.1705G= (F11)	XP_005262879.1:p.Ala569=
XM_005262823.4:c.1531G= (F11)	XP_005262880.1:p.Ala511=
XM_006714137.3:c.1753G= (F11)	XP_006714200.1:p.Ala585=
NM_000128.4:c.1798G= (F11) MANE Select	NP_000119.1:p.Ala600=