Canonical Allele Identifier: CA913103803

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187206846_187206860del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285693_186285707del , CM000666.2:g.186285693_186285707del	GRCh38
NC_000004.11:g.187206847_187206861del , CM000666.1:g.187206847_187206861del	GRCh37
NC_000004.10:g.187443841_187443855del	NCBI36
NG_008051.1:g.24730_24744del , LRG_583:g.24730_24744del

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1360_1374del MANE Select	ENSP00000384957.2:p.Ile454_Thr458del
ENST00000264691.4:c.56_70del
ENST00000264692.8:c.1198_1212del	ENSP00000264692.5:p.Ile400_Thr404del
ENST00000403665.6:c.1360_1374del	ENSP00000384957.2:p.Ile454_Thr458del
NM_000128.3:c.1360_1374del , LRG_583t1:c.1360_1374del	NP_000119.1:p.Ile454_Thr458del
XM_005262821.2:c.1363_1377del	XP_005262878.1:p.Ile455_Thr459del
XM_005262822.2:c.1363_1377del	XP_005262879.1:p.Ile455_Thr459del
XM_005262823.2:c.1093_1107del	XP_005262880.1:p.Ile365_Thr369del
XM_005262824.1:c.1363_1377del	XP_005262881.1:p.Ile455_Thr459del
XM_006714137.1:c.1315_1329del	XP_006714200.1:p.Ile439_Thr443del
XR_938706.1:n.1768_1782del
XR_938707.1:n.1768_1782del
XM_005262821.4:c.1363_1377del	XP_005262878.1:p.Ile455_Thr459del
XM_005262822.4:c.1363_1377del	XP_005262879.1:p.Ile455_Thr459del
XM_005262823.4:c.1093_1107del	XP_005262880.1:p.Ile365_Thr369del
XM_006714137.3:c.1315_1329del	XP_006714200.1:p.Ile439_Thr443del
XR_001741172.2:n.1834_1848del
NM_000128.4:c.1360_1374del MANE Select	NP_000119.1:p.Ile454_Thr458del