Canonical Allele Identifier: CA442638969

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187205298T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284144T>A , CM000666.2:g.186284144T>A	GRCh38
NC_000004.11:g.187205298T>A , CM000666.1:g.187205298T>A	GRCh37
NC_000004.10:g.187442292T>A	NCBI36
NG_008051.1:g.23181T>A , LRG_583:g.23181T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1188T>A MANE Select	ENSP00000384957.2:p.Arg396=
ENST00000264692.8:c.1026T>A	ENSP00000264692.5:p.Arg342=
ENST00000403665.6:c.1188T>A	ENSP00000384957.2:p.Arg396=
NM_000128.3:c.1188T>A , LRG_583t1:c.1188T>A	NP_000119.1:p.Arg396=
XM_005262821.2:c.1191T>A	XP_005262878.1:p.Arg397=
XM_005262822.2:c.1191T>A	XP_005262879.1:p.Arg397=
XM_005262823.2:c.921T>A	XP_005262880.1:p.Arg307=
XM_005262824.1:c.1191T>A	XP_005262881.1:p.Arg397=
XM_006714137.1:c.1143T>A	XP_006714200.1:p.Arg381=
XR_938706.1:n.1596T>A
XR_938707.1:n.1596T>A
XM_005262821.4:c.1191T>A	XP_005262878.1:p.Arg397=
XM_005262822.4:c.1191T>A	XP_005262879.1:p.Arg397=
XM_005262823.4:c.921T>A	XP_005262880.1:p.Arg307=
XM_006714137.3:c.1143T>A	XP_006714200.1:p.Arg381=
XM_017007884.2:c.*2160T>A	XP_016863373.1:n.*2160T>A
XM_017007885.2:c.*56T>A	XP_016863374.1:n.*56T>A
XR_001741172.2:n.1662T>A
NM_000128.4:c.1188T>A MANE Select	NP_000119.1:p.Arg396=