Canonical Allele Identifier: CA1519938800

Gene: F11 F11-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186286418C= , CM000666.2:g.186286418C=	GRCh38
NC_000004.11:g.187207572C= , CM000666.1:g.187207572C=	GRCh37
NC_000004.10:g.187444566C=	NCBI36
NG_008051.1:g.25455C= , LRG_583:g.25455C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1484C= (F11) MANE Select	ENSP00000384957.2:p.Ser495=
ENST00000264691.4:c.176+605C= (F11)
ENST00000264692.8:c.1322C= (F11)	ENSP00000264692.5:p.Ser441=
ENST00000403665.6:c.1484C= (F11)	ENSP00000384957.2:p.Ser495=
NM_000128.3:c.1484C= , LRG_583t1:c.1484C= (F11)	NP_000119.1:p.Ser495=
NR_033900.1:n.1067-152G= (F11-AS1)
XM_005262821.2:c.1487C= (F11)	XP_005262878.1:p.Ser496=
XM_005262822.2:c.1483+605C= (F11)	XP_005262879.1:n.1483+605C=
XM_005262823.2:c.1217C= (F11)	XP_005262880.1:p.Ser406=
XM_005262824.1:c.1484-128C= (F11)	XP_005262881.1:n.1484-128C=
XM_006714137.1:c.1439C= (F11)	XP_006714200.1:p.Ser480=
XR_938706.1:n.1892C= (F11)
XR_938707.1:n.1888+605C= (F11)
XM_005262821.4:c.1487C= (F11)	XP_005262878.1:p.Ser496=
XM_005262822.4:c.1483+605C= (F11)	XP_005262879.1:n.1483+605C=
XM_005262823.4:c.1217C= (F11)	XP_005262880.1:p.Ser406=
XM_006714137.3:c.1439C= (F11)	XP_006714200.1:p.Ser480=
XR_001741172.2:n.1958C= (F11)
NM_000128.4:c.1484C= (F11) MANE Select	NP_000119.1:p.Ser495=