Canonical Allele Identifier: CA358941776

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187205303A>T (hg19) ; chr4:g.186284149A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284149A>T , CM000666.2:g.186284149A>T	GRCh38
NC_000004.11:g.187205303A>T , CM000666.1:g.187205303A>T	GRCh37
NC_000004.10:g.187442297A>T	NCBI36
NG_008051.1:g.23186A>T , LRG_583:g.23186A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1193A>T MANE Select	ENSP00000384957.2:p.Glu398Val
ENST00000264692.8:c.1031A>T	ENSP00000264692.5:p.Glu344Val
ENST00000403665.6:c.1193A>T	ENSP00000384957.2:p.Glu398Val
NM_000128.3:c.1193A>T , LRG_583t1:c.1193A>T	NP_000119.1:p.Glu398Val
XM_005262821.2:c.1196A>T	XP_005262878.1:p.Glu399Val
XM_005262822.2:c.1196A>T	XP_005262879.1:p.Glu399Val
XM_005262823.2:c.926A>T	XP_005262880.1:p.Glu309Val
XM_005262824.1:c.1196A>T	XP_005262881.1:p.Glu399Val
XM_006714137.1:c.1148A>T	XP_006714200.1:p.Glu383Val
XR_938706.1:n.1601A>T
XR_938707.1:n.1601A>T
XM_005262821.4:c.1196A>T	XP_005262878.1:p.Glu399Val
XM_005262822.4:c.1196A>T	XP_005262879.1:p.Glu399Val
XM_005262823.4:c.926A>T	XP_005262880.1:p.Glu309Val
XM_006714137.3:c.1148A>T	XP_006714200.1:p.Glu383Val
XM_017007884.2:c.*2165A>T	XP_016863373.1:n.*2165A>T
XM_017007885.2:c.*61A>T	XP_016863374.1:n.*61A>T
XR_001741172.2:n.1667A>T
NM_000128.4:c.1193A>T MANE Select	NP_000119.1:p.Glu398Val