Canonical Allele Identifier: CA913103805

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187206957dup (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285803dup , CM000666.2:g.186285803dup	GRCh38
NC_000004.11:g.187206957dup , CM000666.1:g.187206957dup	GRCh37
NC_000004.10:g.187443951dup	NCBI36
NG_008051.1:g.24840dup , LRG_583:g.24840dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1470dup MANE Select	ENSP00000384957.2:p.Asn491GlufsTer17
ENST00000264691.4:c.166dup
ENST00000264692.8:c.1308dup	ENSP00000264692.5:p.Asn437GlufsTer17
ENST00000403665.6:c.1470dup	ENSP00000384957.2:p.Asn491GlufsTer17
NM_000128.3:c.1470dup , LRG_583t1:c.1470dup	NP_000119.1:p.Asn491GlufsTer17
XM_005262821.2:c.1473dup	XP_005262878.1:p.Asn492GlufsTer17
XM_005262822.2:c.1473dup	XP_005262879.1:p.Asn492GlufsTer?
XM_005262823.2:c.1203dup	XP_005262880.1:p.Asn402GlufsTer17
XM_005262824.1:c.1473dup	XP_005262881.1:p.Asn492GlufsTer19
XM_006714137.1:c.1425dup	XP_006714200.1:p.Asn476GlufsTer17
XR_938706.1:n.1878dup
XR_938707.1:n.1878dup
XM_005262821.4:c.1473dup	XP_005262878.1:p.Asn492GlufsTer17
XM_005262822.4:c.1473dup	XP_005262879.1:p.Asn492GlufsTer?
XM_005262823.4:c.1203dup	XP_005262880.1:p.Asn402GlufsTer17
XM_006714137.3:c.1425dup	XP_006714200.1:p.Asn476GlufsTer17
XR_001741172.2:n.1944dup
NM_000128.4:c.1470dup MANE Select	NP_000119.1:p.Asn491GlufsTer17