Canonical Allele Identifier: CA1071927529

Gene: F11 F11-AS1

Linked Data

• dbSNP Id: rs1741219985
• gnomAD v3: 4-186286520-ATGT-A
• gnomAD v4: 4-186286520-ATGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186286525_186286527del , CM000666.2:g.186286525_186286527del	GRCh38
NC_000004.11:g.187207679_187207681del , CM000666.1:g.187207679_187207681del	GRCh37
NC_000004.10:g.187444673_187444675del	NCBI36
NG_008051.1:g.25562_25564del , LRG_583:g.25562_25564del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1576+15_1576+17del (F11) MANE Select	ENSP00000384957.2:n.1576+15_1576+17del
ENST00000264691.4:c.176+712_176+714del (F11)
ENST00000264692.8:c.1414+15_1414+17del (F11)	ENSP00000264692.5:n.1414+15_1414+17del
ENST00000403665.6:c.1576+15_1576+17del (F11)	ENSP00000384957.2:n.1576+15_1576+17del
NM_000128.3:c.1576+15_1576+17del , LRG_583t1:c.1576+15_1576+17del (F11)	NP_000119.1:n.1576+15_1576+17del
NR_033900.1:n.1067-257_1067-255del (F11-AS1)
XM_005262821.2:c.1579+15_1579+17del (F11)	XP_005262878.1:n.1579+15_1579+17del
XM_005262822.2:c.1483+712_1483+714del (F11)	XP_005262879.1:n.1483+712_1483+714del
XM_005262823.2:c.1309+15_1309+17del (F11)	XP_005262880.1:n.1309+15_1309+17del
XM_005262824.1:c.1484-21_1484-19del (F11)	XP_005262881.1:n.1484-21_1484-19del
XM_006714137.1:c.1531+15_1531+17del (F11)	XP_006714200.1:n.1531+15_1531+17del
XR_938706.1:n.1984+15_1984+17del (F11)
XR_938707.1:n.1888+712_1888+714del (F11)
XM_005262821.4:c.1579+15_1579+17del (F11)	XP_005262878.1:n.1579+15_1579+17del
XM_005262822.4:c.1483+712_1483+714del (F11)	XP_005262879.1:n.1483+712_1483+714del
XM_005262823.4:c.1309+15_1309+17del (F11)	XP_005262880.1:n.1309+15_1309+17del
XM_006714137.3:c.1531+15_1531+17del (F11)	XP_006714200.1:n.1531+15_1531+17del
NM_000128.4:c.1576+15_1576+17del (F11) MANE Select	NP_000119.1:n.1576+15_1576+17del