Canonical Allele Identifier: CA1519937771

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284163G= , CM000666.2:g.186284163G=	GRCh38
NC_000004.11:g.187205317G= , CM000666.1:g.187205317G=	GRCh37
NC_000004.10:g.187442311G=	NCBI36
NG_008051.1:g.23200G= , LRG_583:g.23200G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1207G= MANE Select	ENSP00000384957.2:p.Val403=
ENST00000264692.8:c.1045G=	ENSP00000264692.5:p.Val349=
ENST00000403665.6:c.1207G=	ENSP00000384957.2:p.Val403=
NM_000128.3:c.1207G= , LRG_583t1:c.1207G=	NP_000119.1:p.Val403=
XM_005262821.2:c.1210G=	XP_005262878.1:p.Val404=
XM_005262822.2:c.1210G=	XP_005262879.1:p.Val404=
XM_005262823.2:c.940G=	XP_005262880.1:p.Val314=
XM_005262824.1:c.1210G=	XP_005262881.1:p.Val404=
XM_006714137.1:c.1162G=	XP_006714200.1:p.Val388=
XR_938706.1:n.1615G=
XR_938707.1:n.1615G=
XM_005262821.4:c.1210G=	XP_005262878.1:p.Val404=
XM_005262822.4:c.1210G=	XP_005262879.1:p.Val404=
XM_005262823.4:c.940G=	XP_005262880.1:p.Val314=
XM_006714137.3:c.1162G=	XP_006714200.1:p.Val388=
XM_017007884.2:c.*2179G=	XP_016863373.1:n.*2179G=
XM_017007885.2:c.*75G=	XP_016863374.1:n.*75G=
XR_001741172.2:n.1681G=
NM_000128.4:c.1207G= MANE Select	NP_000119.1:p.Val403=