Canonical Allele Identifier: CA112103797

Gene: F11

Linked Data

• dbSNP Id: rs35414557
• MyVariant Identifiers: chr4:g.187206931_187206932insC (hg19) ; chr4:g.186285777_186285778insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285779dup , CM000666.2:g.186285779dup	GRCh38
NC_000004.11:g.187206933dup , CM000666.1:g.187206933dup	GRCh37
NC_000004.10:g.187443927dup	NCBI36
NG_008051.1:g.24816dup , LRG_583:g.24816dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1446dup MANE Select	ENSP00000384957.2:p.Leu484ValfsTer24
ENST00000264691.4:c.142dup
ENST00000264692.8:c.1284dup	ENSP00000264692.5:p.Leu430ValfsTer24
ENST00000403665.6:c.1446dup	ENSP00000384957.2:p.Leu484ValfsTer24
NM_000128.3:c.1446dup , LRG_583t1:c.1446dup	NP_000119.1:p.Leu484ValfsTer24
XM_005262821.2:c.1449dup	XP_005262878.1:p.Leu485ValfsTer24
XM_005262822.2:c.1449dup	XP_005262879.1:p.Leu485ValfsTer?
XM_005262823.2:c.1179dup	XP_005262880.1:p.Leu395ValfsTer24
XM_005262824.1:c.1449dup	XP_005262881.1:p.Leu485ValfsTer26
XM_006714137.1:c.1401dup	XP_006714200.1:p.Leu469ValfsTer24
XR_938706.1:n.1854dup
XR_938707.1:n.1854dup
XM_005262821.4:c.1449dup	XP_005262878.1:p.Leu485ValfsTer24
XM_005262822.4:c.1449dup	XP_005262879.1:p.Leu485ValfsTer?
XM_005262823.4:c.1179dup	XP_005262880.1:p.Leu395ValfsTer24
XM_006714137.3:c.1401dup	XP_006714200.1:p.Leu469ValfsTer24
XR_001741172.2:n.1920dup
NM_000128.4:c.1446dup MANE Select	NP_000119.1:p.Leu484ValfsTer24