Canonical Allele Identifier: CA2672903479

Gene: F11 F11-AS1

Linked Data

• gnomAD v4: 4-186286268-TGAGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186286273_186286276del , CM000666.2:g.186286273_186286276del	GRCh38
NC_000004.11:g.187207427_187207430del , CM000666.1:g.187207427_187207430del	GRCh37
NC_000004.10:g.187444421_187444424del	NCBI36
NG_008051.1:g.25310_25313del , LRG_583:g.25310_25313del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1481-142_1481-139del (F11) MANE Select	ENSP00000384957.2:n.1481-142_1481-139del
ENST00000264691.4:c.176+460_176+463del (F11)
ENST00000264692.8:c.1319-142_1319-139del (F11)	ENSP00000264692.5:n.1319-142_1319-139del
ENST00000403665.6:c.1481-142_1481-139del (F11)	ENSP00000384957.2:n.1481-142_1481-139del
NM_000128.3:c.1481-142_1481-139del , LRG_583t1:c.1481-142_1481-139del (F11)	NP_000119.1:n.1481-142_1481-139del
NR_033900.1:n.1067-6_1067-3del (F11-AS1)
XM_005262821.2:c.1484-142_1484-139del (F11)	XP_005262878.1:n.1484-142_1484-139del
XM_005262822.2:c.1483+460_1483+463del (F11)	XP_005262879.1:n.1483+460_1483+463del
XM_005262823.2:c.1214-142_1214-139del (F11)	XP_005262880.1:n.1214-142_1214-139del
XM_005262824.1:c.1484-273_1484-270del (F11)	XP_005262881.1:n.1484-273_1484-270del
XM_006714137.1:c.1436-142_1436-139del (F11)	XP_006714200.1:n.1436-142_1436-139del
XR_938706.1:n.1889-142_1889-139del (F11)
XR_938707.1:n.1888+460_1888+463del (F11)
XM_005262821.4:c.1484-142_1484-139del (F11)	XP_005262878.1:n.1484-142_1484-139del
XM_005262822.4:c.1483+460_1483+463del (F11)	XP_005262879.1:n.1483+460_1483+463del
XM_005262823.4:c.1214-142_1214-139del (F11)	XP_005262880.1:n.1214-142_1214-139del
XM_006714137.3:c.1436-142_1436-139del (F11)	XP_006714200.1:n.1436-142_1436-139del
XR_001741172.2:n.1955-142_1955-139del (F11)
NM_000128.4:c.1481-142_1481-139del (F11) MANE Select	NP_000119.1:n.1481-142_1481-139del