Canonical Allele Identifier: CA2672902602

Gene: F11

Linked Data

• gnomAD v4: 4-186280622-ATTCCATGC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280626_186280633del , CM000666.2:g.186280626_186280633del	GRCh38
NC_000004.11:g.187201780_187201787del , CM000666.1:g.187201780_187201787del	GRCh37
NC_000004.10:g.187438774_187438781del	NCBI36
NG_008051.1:g.19663_19670del , LRG_583:g.19663_19670del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1135+46_1135+53del MANE Select	ENSP00000384957.2:n.1135+46_1135+53del
ENST00000264692.8:c.973+46_973+53del	ENSP00000264692.5:n.973+46_973+53del
ENST00000403665.6:c.1135+46_1135+53del	ENSP00000384957.2:n.1135+46_1135+53del
ENST00000452239.1:c.582+46_582+53del
NM_000128.3:c.1135+46_1135+53del , LRG_583t1:c.1135+46_1135+53del	NP_000119.1:n.1135+46_1135+53del
XM_005262821.2:c.1138+46_1138+53del	XP_005262878.1:n.1138+46_1138+53del
XM_005262822.2:c.1138+46_1138+53del	XP_005262879.1:n.1138+46_1138+53del
XM_005262823.2:c.868+46_868+53del	XP_005262880.1:n.868+46_868+53del
XM_005262824.1:c.1138+46_1138+53del	XP_005262881.1:n.1138+46_1138+53del
XM_006714137.1:c.1090+46_1090+53del	XP_006714200.1:n.1090+46_1090+53del
XR_938706.1:n.1490+46_1490+53del
XR_938707.1:n.1490+46_1490+53del
XM_005262821.4:c.1138+46_1138+53del	XP_005262878.1:n.1138+46_1138+53del
XM_005262822.4:c.1138+46_1138+53del	XP_005262879.1:n.1138+46_1138+53del
XM_005262823.4:c.868+46_868+53del	XP_005262880.1:n.868+46_868+53del
XM_006714137.3:c.1090+46_1090+53del	XP_006714200.1:n.1090+46_1090+53del
XM_017007884.2:c.1138+46_1138+53del	XP_016863373.1:n.1138+46_1138+53del
XM_017007885.2:c.1138+46_1138+53del	XP_016863374.1:n.1138+46_1138+53del
XM_017007886.2:c.1135+46_1135+53del	XP_016863375.1:n.1135+46_1135+53del
XR_001741172.2:n.1556+46_1556+53del
NM_000128.4:c.1135+46_1135+53del MANE Select	NP_000119.1:n.1135+46_1135+53del