Canonical Allele Identifier: CA1519927202

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186266341C= , CM000666.2:g.186266341C=	GRCh38
NC_000004.11:g.187187495C= , CM000666.1:g.187187495C=	GRCh37
NC_000004.10:g.187424489C=	NCBI36
NG_008051.1:g.5378C= , LRG_583:g.5378C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.-2+46C= MANE Select	ENSP00000384957.2:n.-2+46C=
ENST00000264692.8:c.-2+46C=	ENSP00000264692.5:n.-2+46C=
ENST00000403665.6:c.-2+46C=	ENSP00000384957.2:n.-2+46C=
ENST00000492972.6:c.-2+46C=	ENSP00000424479.1:n.-2+46C=
NM_000128.3:c.-2+46C= , LRG_583t1:c.-2+46C=	NP_000119.1:n.-2+46C=
XM_005262821.2:c.-2+46C=	XP_005262878.1:n.-2+46C=
XM_005262822.2:c.-2+46C=	XP_005262879.1:n.-2+46C=
XM_005262823.2:c.-2+46C=	XP_005262880.1:n.-2+46C=
XM_005262824.1:c.-2+46C=	XP_005262881.1:n.-2+46C=
XM_006714137.1:c.-2+46C=	XP_006714200.1:n.-2+46C=
XR_938706.1:n.351+46C=
XR_938707.1:n.351+46C=
NM_001354804.1:c.-2+46C=	NP_001341733.1:n.-2+46C=
XM_005262821.4:c.-2+46C=	XP_005262878.1:n.-2+46C=
XM_005262822.4:c.-2+46C=	XP_005262879.1:n.-2+46C=
XM_005262823.4:c.-2+46C=	XP_005262880.1:n.-2+46C=
XM_006714137.3:c.-2+46C=	XP_006714200.1:n.-2+46C=
XM_017007884.2:c.-2+46C=	XP_016863373.1:n.-2+46C=
XM_017007885.2:c.-2+46C=	XP_016863374.1:n.-2+46C=
XM_017007886.2:c.-2+46C=	XP_016863375.1:n.-2+46C=
XR_001741172.2:n.332+46C=
NM_000128.4:c.-2+46C= MANE Select	NP_000119.1:n.-2+46C=
NM_001354804.2:c.-2+46C=	NP_001341733.1:n.-2+46C=