Canonical Allele Identifier: CA2672901581

Gene: F11

Linked Data

• gnomAD v4: 4-186274301-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186274303del , CM000666.2:g.186274303del	GRCh38
NC_000004.11:g.187195457del , CM000666.1:g.187195457del	GRCh37
NC_000004.10:g.187432451del	NCBI36
NG_008051.1:g.13340del , LRG_583:g.13340del

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.485+28del MANE Select	ENSP00000384957.2:n.485+28del
ENST00000264692.8:c.323+1128del	ENSP00000264692.5:n.323+1128del
ENST00000403665.6:c.485+28del	ENSP00000384957.2:n.485+28del
ENST00000492972.6:c.*24del	ENSP00000424479.1:n.*24del
ENST00000514715.1:n.385del
NM_000128.3:c.485+28del , LRG_583t1:c.485+28del	NP_000119.1:n.485+28del
XM_005262821.2:c.485+28del	XP_005262878.1:n.485+28del
XM_005262822.2:c.485+28del	XP_005262879.1:n.485+28del
XM_005262823.2:c.485+28del	XP_005262880.1:n.485+28del
XM_005262824.1:c.485+28del	XP_005262881.1:n.485+28del
XM_006714137.1:c.485+28del	XP_006714200.1:n.485+28del
XR_938706.1:n.837+28del
XR_938707.1:n.837+28del
NM_001354804.1:c.*24del	NP_001341733.1:n.*24del
XM_005262821.4:c.485+28del	XP_005262878.1:n.485+28del
XM_005262822.4:c.485+28del	XP_005262879.1:n.485+28del
XM_005262823.4:c.485+28del	XP_005262880.1:n.485+28del
XM_006714137.3:c.485+28del	XP_006714200.1:n.485+28del
XM_017007884.2:c.485+28del	XP_016863373.1:n.485+28del
XM_017007885.2:c.485+28del	XP_016863374.1:n.485+28del
XM_017007886.2:c.485+28del	XP_016863375.1:n.485+28del
XR_001741172.2:n.818+28del
NM_000128.4:c.485+28del MANE Select	NP_000119.1:n.485+28del
NM_001354804.2:c.*24del	NP_001341733.1:n.*24del