Canonical Allele Identifier: CA1519933202

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186274082_186274088delinsGGAAGGT , CM000666.2:g.186274082_186274088delinsGGAAGGT	GRCh38
NC_000004.11:g.187195236_187195242delinsGGAAGGT , CM000666.1:g.187195236_187195242delinsGGAAGGT	GRCh37
NC_000004.10:g.187432230_187432236delinsGGAAGGT	NCBI36
NG_008051.1:g.13119_13125delinsGGAAGGT , LRG_583:g.13119_13125delinsGGAAGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.326-34_326-28delinsGGAAGGT MANE Select	ENSP00000384957.2:n.326-34_326-28delinsGGAAGGT
ENST00000264692.8:c.323+907_323+913delinsGGAAGGT	ENSP00000264692.5:n.323+907_323+913delinsGGAAGGT
ENST00000403665.6:c.326-34_326-28delinsGGAAGGT	ENSP00000384957.2:n.326-34_326-28delinsGGAAGGT
ENST00000492972.6:c.326-34_326-28delinsGGAAGGT	ENSP00000424479.1:n.326-34_326-28delinsGGAAGGT
ENST00000514715.1:n.198-34_198-28delinsGGAAGGT
NM_000128.3:c.326-34_326-28delinsGGAAGGT , LRG_583t1:c.326-34_326-28delinsGGAAGGT	NP_000119.1:n.326-34_326-28delinsGGAAGGT
XM_005262821.2:c.326-34_326-28delinsGGAAGGT	XP_005262878.1:n.326-34_326-28delinsGGAAGGT
XM_005262822.2:c.326-34_326-28delinsGGAAGGT	XP_005262879.1:n.326-34_326-28delinsGGAAGGT
XM_005262823.2:c.326-34_326-28delinsGGAAGGT	XP_005262880.1:n.326-34_326-28delinsGGAAGGT
XM_005262824.1:c.326-34_326-28delinsGGAAGGT	XP_005262881.1:n.326-34_326-28delinsGGAAGGT
XM_006714137.1:c.326-34_326-28delinsGGAAGGT	XP_006714200.1:n.326-34_326-28delinsGGAAGGT
XR_938706.1:n.678-34_678-28delinsGGAAGGT
XR_938707.1:n.678-34_678-28delinsGGAAGGT
NM_001354804.1:c.326-34_326-28delinsGGAAGGT	NP_001341733.1:n.326-34_326-28delinsGGAAGGT
XM_005262821.4:c.326-34_326-28delinsGGAAGGT	XP_005262878.1:n.326-34_326-28delinsGGAAGGT
XM_005262822.4:c.326-34_326-28delinsGGAAGGT	XP_005262879.1:n.326-34_326-28delinsGGAAGGT
XM_005262823.4:c.326-34_326-28delinsGGAAGGT	XP_005262880.1:n.326-34_326-28delinsGGAAGGT
XM_006714137.3:c.326-34_326-28delinsGGAAGGT	XP_006714200.1:n.326-34_326-28delinsGGAAGGT
XM_017007884.2:c.326-34_326-28delinsGGAAGGT	XP_016863373.1:n.326-34_326-28delinsGGAAGGT
XM_017007885.2:c.326-34_326-28delinsGGAAGGT	XP_016863374.1:n.326-34_326-28delinsGGAAGGT
XM_017007886.2:c.326-34_326-28delinsGGAAGGT	XP_016863375.1:n.326-34_326-28delinsGGAAGGT
XR_001741172.2:n.659-34_659-28delinsGGAAGGT
NM_000128.4:c.326-34_326-28delinsGGAAGGT MANE Select	NP_000119.1:n.326-34_326-28delinsGGAAGGT
NM_001354804.2:c.326-34_326-28delinsGGAAGGT	NP_001341733.1:n.326-34_326-28delinsGGAAGGT