Canonical Allele Identifier: CA2672903429

Gene: F11

Linked Data

• gnomAD v4: 4-186283970-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186283972del , CM000666.2:g.186283972del	GRCh38
NC_000004.11:g.187205126del , CM000666.1:g.187205126del	GRCh37
NC_000004.10:g.187442120del	NCBI36
NG_008051.1:g.23009del , LRG_583:g.23009del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1136-120del MANE Select	ENSP00000384957.2:n.1136-120del
ENST00000264692.8:c.974-120del	ENSP00000264692.5:n.974-120del
ENST00000403665.6:c.1136-120del	ENSP00000384957.2:n.1136-120del
NM_000128.3:c.1136-120del , LRG_583t1:c.1136-120del	NP_000119.1:n.1136-120del
XM_005262821.2:c.1139-120del	XP_005262878.1:n.1139-120del
XM_005262822.2:c.1139-120del	XP_005262879.1:n.1139-120del
XM_005262823.2:c.869-120del	XP_005262880.1:n.869-120del
XM_005262824.1:c.1139-120del	XP_005262881.1:n.1139-120del
XM_006714137.1:c.1091-120del	XP_006714200.1:n.1091-120del
XR_938706.1:n.1544-120del
XR_938707.1:n.1544-120del
XM_005262821.4:c.1139-120del	XP_005262878.1:n.1139-120del
XM_005262822.4:c.1139-120del	XP_005262879.1:n.1139-120del
XM_005262823.4:c.869-120del	XP_005262880.1:n.869-120del
XM_006714137.3:c.1091-120del	XP_006714200.1:n.1091-120del
XM_017007884.2:c.*1988del	XP_016863373.1:n.*1988del
XM_017007885.2:c.*4-120del	XP_016863374.1:n.*4-120del
XR_001741172.2:n.1610-120del
NM_000128.4:c.1136-120del MANE Select	NP_000119.1:n.1136-120del