Canonical Allele Identifier: CA1519933197

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186274078_186274081delinsATCT , CM000666.2:g.186274078_186274081delinsATCT	GRCh38
NC_000004.11:g.187195232_187195235delinsATCT , CM000666.1:g.187195232_187195235delinsATCT	GRCh37
NC_000004.10:g.187432226_187432229delinsATCT	NCBI36
NG_008051.1:g.13115_13118delinsATCT , LRG_583:g.13115_13118delinsATCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.326-38_326-35delinsATCT MANE Select	ENSP00000384957.2:n.326-38_326-35delinsATCT
ENST00000264692.8:c.323+903_323+906delinsATCT	ENSP00000264692.5:n.323+903_323+906delinsATCT
ENST00000403665.6:c.326-38_326-35delinsATCT	ENSP00000384957.2:n.326-38_326-35delinsATCT
ENST00000492972.6:c.326-38_326-35delinsATCT	ENSP00000424479.1:n.326-38_326-35delinsATCT
ENST00000514715.1:n.198-38_198-35delinsATCT
NM_000128.3:c.326-38_326-35delinsATCT , LRG_583t1:c.326-38_326-35delinsATCT	NP_000119.1:n.326-38_326-35delinsATCT
XM_005262821.2:c.326-38_326-35delinsATCT	XP_005262878.1:n.326-38_326-35delinsATCT
XM_005262822.2:c.326-38_326-35delinsATCT	XP_005262879.1:n.326-38_326-35delinsATCT
XM_005262823.2:c.326-38_326-35delinsATCT	XP_005262880.1:n.326-38_326-35delinsATCT
XM_005262824.1:c.326-38_326-35delinsATCT	XP_005262881.1:n.326-38_326-35delinsATCT
XM_006714137.1:c.326-38_326-35delinsATCT	XP_006714200.1:n.326-38_326-35delinsATCT
XR_938706.1:n.678-38_678-35delinsATCT
XR_938707.1:n.678-38_678-35delinsATCT
NM_001354804.1:c.326-38_326-35delinsATCT	NP_001341733.1:n.326-38_326-35delinsATCT
XM_005262821.4:c.326-38_326-35delinsATCT	XP_005262878.1:n.326-38_326-35delinsATCT
XM_005262822.4:c.326-38_326-35delinsATCT	XP_005262879.1:n.326-38_326-35delinsATCT
XM_005262823.4:c.326-38_326-35delinsATCT	XP_005262880.1:n.326-38_326-35delinsATCT
XM_006714137.3:c.326-38_326-35delinsATCT	XP_006714200.1:n.326-38_326-35delinsATCT
XM_017007884.2:c.326-38_326-35delinsATCT	XP_016863373.1:n.326-38_326-35delinsATCT
XM_017007885.2:c.326-38_326-35delinsATCT	XP_016863374.1:n.326-38_326-35delinsATCT
XM_017007886.2:c.326-38_326-35delinsATCT	XP_016863375.1:n.326-38_326-35delinsATCT
XR_001741172.2:n.659-38_659-35delinsATCT
NM_000128.4:c.326-38_326-35delinsATCT MANE Select	NP_000119.1:n.326-38_326-35delinsATCT
NM_001354804.2:c.326-38_326-35delinsATCT	NP_001341733.1:n.326-38_326-35delinsATCT