Canonical Allele Identifier: CA1519933463

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186274644T= , CM000666.2:g.186274644T=	GRCh38
NC_000004.11:g.187195798T= , CM000666.1:g.187195798T=	GRCh37
NC_000004.10:g.187432792T=	NCBI36
NG_008051.1:g.13681T= , LRG_583:g.13681T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.485+369T= MANE Select	ENSP00000384957.2:n.485+369T=
ENST00000264692.8:c.324-1143T=	ENSP00000264692.5:n.324-1143T=
ENST00000403665.6:c.485+369T=	ENSP00000384957.2:n.485+369T=
ENST00000492972.6:c.*365T=	ENSP00000424479.1:n.*365T=
NM_000128.3:c.485+369T= , LRG_583t1:c.485+369T=	NP_000119.1:n.485+369T=
XM_005262821.2:c.485+369T=	XP_005262878.1:n.485+369T=
XM_005262822.2:c.485+369T=	XP_005262879.1:n.485+369T=
XM_005262823.2:c.485+369T=	XP_005262880.1:n.485+369T=
XM_005262824.1:c.485+369T=	XP_005262881.1:n.485+369T=
XM_006714137.1:c.485+369T=	XP_006714200.1:n.485+369T=
XR_938706.1:n.837+369T=
XR_938707.1:n.837+369T=
NM_001354804.1:c.*365T=	NP_001341733.1:n.*365T=
XM_005262821.4:c.485+369T=	XP_005262878.1:n.485+369T=
XM_005262822.4:c.485+369T=	XP_005262879.1:n.485+369T=
XM_005262823.4:c.485+369T=	XP_005262880.1:n.485+369T=
XM_006714137.3:c.485+369T=	XP_006714200.1:n.485+369T=
XM_017007884.2:c.485+369T=	XP_016863373.1:n.485+369T=
XM_017007885.2:c.485+369T=	XP_016863374.1:n.485+369T=
XM_017007886.2:c.485+369T=	XP_016863375.1:n.485+369T=
XR_001741172.2:n.818+369T=
NM_000128.4:c.485+369T= MANE Select	NP_000119.1:n.485+369T=
NM_001354804.2:c.*365T=	NP_001341733.1:n.*365T=