Canonical Allele Identifier: CA2672902483

Gene: F11

Linked Data

• gnomAD v4: 4-186280390-GCCATATGAAGGGTTATGCAGACA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280393_186280415del , CM000666.2:g.186280393_186280415del	GRCh38
NC_000004.11:g.187201547_187201569del , CM000666.1:g.187201547_187201569del	GRCh37
NC_000004.10:g.187438541_187438563del	NCBI36
NG_008051.1:g.19430_19452del , LRG_583:g.19430_19452del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1028+8_1028+30del MANE Select	ENSP00000384957.2:n.1028+8_1028+30del
ENST00000264692.8:c.866+8_866+30del	ENSP00000264692.5:n.866+8_866+30del
ENST00000403665.6:c.1028+8_1028+30del	ENSP00000384957.2:n.1028+8_1028+30del
ENST00000452239.1:c.475+8_475+30del
NM_000128.3:c.1028+8_1028+30del , LRG_583t1:c.1028+8_1028+30del	NP_000119.1:n.1028+8_1028+30del
XM_005262821.2:c.1028+8_1028+30del	XP_005262878.1:n.1028+8_1028+30del
XM_005262822.2:c.1028+8_1028+30del	XP_005262879.1:n.1028+8_1028+30del
XM_005262823.2:c.758+8_758+30del	XP_005262880.1:n.758+8_758+30del
XM_005262824.1:c.1028+8_1028+30del	XP_005262881.1:n.1028+8_1028+30del
XM_006714137.1:c.980+8_980+30del	XP_006714200.1:n.980+8_980+30del
XR_938706.1:n.1380+8_1380+30del
XR_938707.1:n.1380+8_1380+30del
XM_005262821.4:c.1028+8_1028+30del	XP_005262878.1:n.1028+8_1028+30del
XM_005262822.4:c.1028+8_1028+30del	XP_005262879.1:n.1028+8_1028+30del
XM_005262823.4:c.758+8_758+30del	XP_005262880.1:n.758+8_758+30del
XM_006714137.3:c.980+8_980+30del	XP_006714200.1:n.980+8_980+30del
XM_017007884.2:c.1028+8_1028+30del	XP_016863373.1:n.1028+8_1028+30del
XM_017007885.2:c.1028+8_1028+30del	XP_016863374.1:n.1028+8_1028+30del
XM_017007886.2:c.1028+8_1028+30del	XP_016863375.1:n.1028+8_1028+30del
XR_001741172.2:n.1369_1391del
NM_000128.4:c.1028+8_1028+30del MANE Select	NP_000119.1:n.1028+8_1028+30del