Canonical Allele Identifier: CA2672904201

Gene: F11 F11-AS1

Linked Data

• gnomAD v4: 4-186288775-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288776del , CM000666.2:g.186288776del	GRCh38
NC_000004.11:g.187209930del , CM000666.1:g.187209930del	GRCh37
NC_000004.10:g.187446924del	NCBI36
NG_008051.1:g.27813del , LRG_583:g.27813del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.*162del (F11) MANE Select	ENSP00000384957.2:n.*162del
ENST00000264691.4:c.640del (F11)
ENST00000264692.8:c.*162del (F11)	ENSP00000264692.5:n.*162del
ENST00000403665.6:c.*162del (F11)	ENSP00000384957.2:n.*162del
ENST00000503841.1:n.559del (F11)
NM_000128.3:c.*162del , LRG_583t1:c.*162del (F11)	NP_000119.1:n.*162del
NR_033900.1:n.718del (F11-AS1)
XM_005262821.2:c.*162del (F11)	XP_005262878.1:n.*162del
XM_005262822.2:c.*162del (F11)	XP_005262879.1:n.*162del
XM_005262823.2:c.*162del (F11)	XP_005262880.1:n.*162del
XM_006714137.1:c.*162del (F11)	XP_006714200.1:n.*162del
XM_005262821.4:c.*162del (F11)	XP_005262878.1:n.*162del
XM_005262822.4:c.*162del (F11)	XP_005262879.1:n.*162del
XM_005262823.4:c.*162del (F11)	XP_005262880.1:n.*162del
XM_006714137.3:c.*162del (F11)	XP_006714200.1:n.*162del
NM_000128.4:c.*162del (F11) MANE Select	NP_000119.1:n.*162del