Canonical Allele Identifier: CA913103802

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187206815_187206816del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285663_186285664del , CM000666.2:g.186285663_186285664del	GRCh38
NC_000004.11:g.187206817_187206818del , CM000666.1:g.187206817_187206818del	GRCh37
NC_000004.10:g.187443811_187443812del	NCBI36
NG_008051.1:g.24700_24701del , LRG_583:g.24700_24701del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1330_1331del MANE Select	ENSP00000384957.2:p.Val444LeufsTer9
ENST00000264691.4:c.26_27del
ENST00000264692.8:c.1168_1169del	ENSP00000264692.5:p.Val390LeufsTer9
ENST00000403665.6:c.1330_1331del	ENSP00000384957.2:p.Val444LeufsTer9
NM_000128.3:c.1330_1331del , LRG_583t1:c.1330_1331del	NP_000119.1:p.Val444LeufsTer9
XM_005262821.2:c.1333_1334del	XP_005262878.1:p.Val445LeufsTer9
XM_005262822.2:c.1333_1334del	XP_005262879.1:p.Val445LeufsTer9
XM_005262823.2:c.1063_1064del	XP_005262880.1:p.Val355LeufsTer9
XM_005262824.1:c.1333_1334del	XP_005262881.1:p.Val445LeufsTer9
XM_006714137.1:c.1285_1286del	XP_006714200.1:p.Val429LeufsTer9
XR_938706.1:n.1738_1739del
XR_938707.1:n.1738_1739del
XM_005262821.4:c.1333_1334del	XP_005262878.1:p.Val445LeufsTer9
XM_005262822.4:c.1333_1334del	XP_005262879.1:p.Val445LeufsTer9
XM_005262823.4:c.1063_1064del	XP_005262880.1:p.Val355LeufsTer9
XM_006714137.3:c.1285_1286del	XP_006714200.1:p.Val429LeufsTer9
XR_001741172.2:n.1804_1805del
NM_000128.4:c.1330_1331del MANE Select	NP_000119.1:p.Val444LeufsTer9