Canonical Allele Identifier: CA913103804

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187206861_187206865del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285707_186285711del , CM000666.2:g.186285707_186285711del	GRCh38
NC_000004.11:g.187206861_187206865del , CM000666.1:g.187206861_187206865del	GRCh37
NC_000004.10:g.187443855_187443859del	NCBI36
NG_008051.1:g.24744_24748del , LRG_583:g.24744_24748del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1374_1378del MANE Select	ENSP00000384957.2:p.Ser459LeufsTer10
ENST00000264691.4:c.70_74del
ENST00000264692.8:c.1212_1216del	ENSP00000264692.5:p.Ser405LeufsTer10
ENST00000403665.6:c.1374_1378del	ENSP00000384957.2:p.Ser459LeufsTer10
NM_000128.3:c.1374_1378del , LRG_583t1:c.1374_1378del	NP_000119.1:p.Ser459LeufsTer10
XM_005262821.2:c.1377_1381del	XP_005262878.1:p.Ser460LeufsTer10
XM_005262822.2:c.1377_1381del	XP_005262879.1:p.Ser460LeufsTer10
XM_005262823.2:c.1107_1111del	XP_005262880.1:p.Ser370LeufsTer10
XM_005262824.1:c.1377_1381del	XP_005262881.1:p.Ser460LeufsTer10
XM_006714137.1:c.1329_1333del	XP_006714200.1:p.Ser444LeufsTer10
XR_938706.1:n.1782_1786del
XR_938707.1:n.1782_1786del
XM_005262821.4:c.1377_1381del	XP_005262878.1:p.Ser460LeufsTer10
XM_005262822.4:c.1377_1381del	XP_005262879.1:p.Ser460LeufsTer10
XM_005262823.4:c.1107_1111del	XP_005262880.1:p.Ser370LeufsTer10
XM_006714137.3:c.1329_1333del	XP_006714200.1:p.Ser444LeufsTer10
XR_001741172.2:n.1848_1852del
NM_000128.4:c.1374_1378del MANE Select	NP_000119.1:p.Ser459LeufsTer10