Canonical Allele Identifier: CA1519933446

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186274604_186274606delinsTAC , CM000666.2:g.186274604_186274606delinsTAC	GRCh38
NC_000004.11:g.187195758_187195760delinsTAC , CM000666.1:g.187195758_187195760delinsTAC	GRCh37
NC_000004.10:g.187432752_187432754delinsTAC	NCBI36
NG_008051.1:g.13641_13643delinsTAC , LRG_583:g.13641_13643delinsTAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.485+329_485+331delinsTAC MANE Select	ENSP00000384957.2:n.485+329_485+331delinsTAC
ENST00000264692.8:c.324-1183_324-1181delinsTAC	ENSP00000264692.5:n.324-1183_324-1181delinsTAC
ENST00000403665.6:c.485+329_485+331delinsTAC	ENSP00000384957.2:n.485+329_485+331delinsTAC
ENST00000492972.6:c.*325_*327delinsTAC	ENSP00000424479.1:n.*325_*327delinsTAC
ENST00000514715.1:n.686_688delinsTAC
NM_000128.3:c.485+329_485+331delinsTAC , LRG_583t1:c.485+329_485+331delinsTAC	NP_000119.1:n.485+329_485+331delinsTAC
XM_005262821.2:c.485+329_485+331delinsTAC	XP_005262878.1:n.485+329_485+331delinsTAC
XM_005262822.2:c.485+329_485+331delinsTAC	XP_005262879.1:n.485+329_485+331delinsTAC
XM_005262823.2:c.485+329_485+331delinsTAC	XP_005262880.1:n.485+329_485+331delinsTAC
XM_005262824.1:c.485+329_485+331delinsTAC	XP_005262881.1:n.485+329_485+331delinsTAC
XM_006714137.1:c.485+329_485+331delinsTAC	XP_006714200.1:n.485+329_485+331delinsTAC
XR_938706.1:n.837+329_837+331delinsTAC
XR_938707.1:n.837+329_837+331delinsTAC
NM_001354804.1:c.*325_*327delinsTAC	NP_001341733.1:n.*325_*327delinsTAC
XM_005262821.4:c.485+329_485+331delinsTAC	XP_005262878.1:n.485+329_485+331delinsTAC
XM_005262822.4:c.485+329_485+331delinsTAC	XP_005262879.1:n.485+329_485+331delinsTAC
XM_005262823.4:c.485+329_485+331delinsTAC	XP_005262880.1:n.485+329_485+331delinsTAC
XM_006714137.3:c.485+329_485+331delinsTAC	XP_006714200.1:n.485+329_485+331delinsTAC
XM_017007884.2:c.485+329_485+331delinsTAC	XP_016863373.1:n.485+329_485+331delinsTAC
XM_017007885.2:c.485+329_485+331delinsTAC	XP_016863374.1:n.485+329_485+331delinsTAC
XM_017007886.2:c.485+329_485+331delinsTAC	XP_016863375.1:n.485+329_485+331delinsTAC
XR_001741172.2:n.818+329_818+331delinsTAC
NM_000128.4:c.485+329_485+331delinsTAC MANE Select	NP_000119.1:n.485+329_485+331delinsTAC
NM_001354804.2:c.*325_*327delinsTAC	NP_001341733.1:n.*325_*327delinsTAC