Canonical Allele Identifier: CA2672901823

Gene: F11

Linked Data

• gnomAD v4: 4-186274699-C-CCTG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186274699_186274700insCTG , CM000666.2:g.186274699_186274700insCTG	GRCh38
NC_000004.11:g.187195853_187195854insCTG , CM000666.1:g.187195853_187195854insCTG	GRCh37
NC_000004.10:g.187432847_187432848insCTG	NCBI36
NG_008051.1:g.13736_13737insCTG , LRG_583:g.13736_13737insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.485+424_485+425insCTG MANE Select	ENSP00000384957.2:n.485+424_485+425insCTG
ENST00000264692.8:c.324-1088_324-1087insCTG	ENSP00000264692.5:n.324-1088_324-1087insCTG
ENST00000403665.6:c.485+424_485+425insCTG	ENSP00000384957.2:n.485+424_485+425insCTG
ENST00000492972.6:c.*420_*421insCTG	ENSP00000424479.1:n.*420_*421insCTG
NM_000128.3:c.485+424_485+425insCTG , LRG_583t1:c.485+424_485+425insCTG	NP_000119.1:n.485+424_485+425insCTG
XM_005262821.2:c.485+424_485+425insCTG	XP_005262878.1:n.485+424_485+425insCTG
XM_005262822.2:c.485+424_485+425insCTG	XP_005262879.1:n.485+424_485+425insCTG
XM_005262823.2:c.485+424_485+425insCTG	XP_005262880.1:n.485+424_485+425insCTG
XM_005262824.1:c.485+424_485+425insCTG	XP_005262881.1:n.485+424_485+425insCTG
XM_006714137.1:c.485+424_485+425insCTG	XP_006714200.1:n.485+424_485+425insCTG
XR_938706.1:n.837+424_837+425insCTG
XR_938707.1:n.837+424_837+425insCTG
NM_001354804.1:c.*420_*421insCTG	NP_001341733.1:n.*420_*421insCTG
XM_005262821.4:c.485+424_485+425insCTG	XP_005262878.1:n.485+424_485+425insCTG
XM_005262822.4:c.485+424_485+425insCTG	XP_005262879.1:n.485+424_485+425insCTG
XM_005262823.4:c.485+424_485+425insCTG	XP_005262880.1:n.485+424_485+425insCTG
XM_006714137.3:c.485+424_485+425insCTG	XP_006714200.1:n.485+424_485+425insCTG
XM_017007884.2:c.485+424_485+425insCTG	XP_016863373.1:n.485+424_485+425insCTG
XM_017007885.2:c.485+424_485+425insCTG	XP_016863374.1:n.485+424_485+425insCTG
XM_017007886.2:c.485+424_485+425insCTG	XP_016863375.1:n.485+424_485+425insCTG
XR_001741172.2:n.818+424_818+425insCTG
NM_000128.4:c.485+424_485+425insCTG MANE Select	NP_000119.1:n.485+424_485+425insCTG
NM_001354804.2:c.*420_*421insCTG	NP_001341733.1:n.*420_*421insCTG