Canonical Allele Identifier: CA1519938548

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285795A= , CM000666.2:g.186285795A=	GRCh38
NC_000004.11:g.187206949A= , CM000666.1:g.187206949A=	GRCh37
NC_000004.10:g.187443943A=	NCBI36
NG_008051.1:g.24832A= , LRG_583:g.24832A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1462A= MANE Select	ENSP00000384957.2:p.Thr488=
ENST00000264691.4:c.158A=
ENST00000264692.8:c.1300A=	ENSP00000264692.5:p.Thr434=
ENST00000403665.6:c.1462A=	ENSP00000384957.2:p.Thr488=
NM_000128.3:c.1462A= , LRG_583t1:c.1462A=	NP_000119.1:p.Thr488=
XM_005262821.2:c.1465A=	XP_005262878.1:p.Thr489=
XM_005262822.2:c.1465A=	XP_005262879.1:p.Thr489=
XM_005262823.2:c.1195A=	XP_005262880.1:p.Thr399=
XM_005262824.1:c.1465A=	XP_005262881.1:p.Thr489=
XM_006714137.1:c.1417A=	XP_006714200.1:p.Thr473=
XR_938706.1:n.1870A=
XR_938707.1:n.1870A=
XM_005262821.4:c.1465A=	XP_005262878.1:p.Thr489=
XM_005262822.4:c.1465A=	XP_005262879.1:p.Thr489=
XM_005262823.4:c.1195A=	XP_005262880.1:p.Thr399=
XM_006714137.3:c.1417A=	XP_006714200.1:p.Thr473=
XR_001741172.2:n.1936A=
NM_000128.4:c.1462A= MANE Select	NP_000119.1:p.Thr488=