Canonical Allele Identifier: CA1519936061

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280426C= , CM000666.2:g.186280426C=	GRCh38
NC_000004.11:g.187201580C= , CM000666.1:g.187201580C=	GRCh37
NC_000004.10:g.187438574C=	NCBI36
NG_008051.1:g.19463C= , LRG_583:g.19463C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1028+41C= MANE Select	ENSP00000384957.2:n.1028+41C=
ENST00000264692.8:c.866+41C=	ENSP00000264692.5:n.866+41C=
ENST00000403665.6:c.1028+41C=	ENSP00000384957.2:n.1028+41C=
ENST00000452239.1:c.475+41C=
NM_000128.3:c.1028+41C= , LRG_583t1:c.1028+41C=	NP_000119.1:n.1028+41C=
XM_005262821.2:c.1028+41C=	XP_005262878.1:n.1028+41C=
XM_005262822.2:c.1028+41C=	XP_005262879.1:n.1028+41C=
XM_005262823.2:c.758+41C=	XP_005262880.1:n.758+41C=
XM_005262824.1:c.1028+41C=	XP_005262881.1:n.1028+41C=
XM_006714137.1:c.980+41C=	XP_006714200.1:n.980+41C=
XR_938706.1:n.1380+41C=
XR_938707.1:n.1380+41C=
XM_005262821.4:c.1028+41C=	XP_005262878.1:n.1028+41C=
XM_005262822.4:c.1028+41C=	XP_005262879.1:n.1028+41C=
XM_005262823.4:c.758+41C=	XP_005262880.1:n.758+41C=
XM_006714137.3:c.980+41C=	XP_006714200.1:n.980+41C=
XM_017007884.2:c.1028+41C=	XP_016863373.1:n.1028+41C=
XM_017007885.2:c.1028+41C=	XP_016863374.1:n.1028+41C=
XM_017007886.2:c.1028+41C=	XP_016863375.1:n.1028+41C=
XR_001741172.2:n.1402C=
NM_000128.4:c.1028+41C= MANE Select	NP_000119.1:n.1028+41C=