Canonical Allele Identifier: CA2580071723

Gene: F11

Linked Data

• ClinVar Variation Id: 1724343
• ClinVar RCV Id: RCV002309611

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285698del , CM000666.2:g.186285698del	GRCh38
NC_000004.11:g.187206852del , CM000666.1:g.187206852del	GRCh37
NC_000004.10:g.187443846del	NCBI36
NG_008051.1:g.24735del , LRG_583:g.24735del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1365del MANE Select	ENSP00000384957.2:p.Glu456ArgfsTer11
ENST00000264691.4:c.61del
ENST00000264692.8:c.1203del	ENSP00000264692.5:p.Glu402ArgfsTer11
ENST00000403665.6:c.1365del	ENSP00000384957.2:p.Glu456ArgfsTer11
NM_000128.3:c.1365del , LRG_583t1:c.1365del	NP_000119.1:p.Glu456ArgfsTer11
XM_005262821.2:c.1368del	XP_005262878.1:p.Glu457ArgfsTer11
XM_005262822.2:c.1368del	XP_005262879.1:p.Glu457ArgfsTer11
XM_005262823.2:c.1098del	XP_005262880.1:p.Glu367ArgfsTer11
XM_005262824.1:c.1368del	XP_005262881.1:p.Glu457ArgfsTer11
XM_006714137.1:c.1320del	XP_006714200.1:p.Glu441ArgfsTer11
XR_938706.1:n.1773del
XR_938707.1:n.1773del
XM_005262821.4:c.1368del	XP_005262878.1:p.Glu457ArgfsTer11
XM_005262822.4:c.1368del	XP_005262879.1:p.Glu457ArgfsTer11
XM_005262823.4:c.1098del	XP_005262880.1:p.Glu367ArgfsTer11
XM_006714137.3:c.1320del	XP_006714200.1:p.Glu441ArgfsTer11
XR_001741172.2:n.1839del
NM_000128.4:c.1365del MANE Select	NP_000119.1:p.Glu456ArgfsTer11