Canonical Allele Identifier: CA1071927986

Gene: F11 F11-AS1

Linked Data

• dbSNP Id: rs1741383462
• gnomAD v3: 4-186288521-GGGCGAA-G
• gnomAD v4: 4-186288521-GGGCGAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288525_186288530del , CM000666.2:g.186288525_186288530del	GRCh38
NC_000004.11:g.187209679_187209684del , CM000666.1:g.187209679_187209684del	GRCh37
NC_000004.10:g.187446673_187446678del	NCBI36
NG_008051.1:g.27562_27567del , LRG_583:g.27562_27567del

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1789_1794del (F11) MANE Select	ENSP00000384957.2:p.Glu597_Gly598del
ENST00000264691.4:c.389_394del (F11)
ENST00000264692.8:c.1627_1632del (F11)	ENSP00000264692.5:p.Glu543_Gly544del
ENST00000403665.6:c.1789_1794del (F11)	ENSP00000384957.2:p.Glu597_Gly598del
ENST00000503841.1:n.308_313del (F11)
NM_000128.3:c.1789_1794del , LRG_583t1:c.1789_1794del (F11)	NP_000119.1:p.Glu597_Gly598del
NR_033900.1:n.967_972del (F11-AS1)
XM_005262821.2:c.1792_1797del (F11)	XP_005262878.1:p.Glu598_Gly599del
XM_005262822.2:c.1696_1701del (F11)	XP_005262879.1:p.Glu566_Gly567del
XM_005262823.2:c.1522_1527del (F11)	XP_005262880.1:p.Glu508_Gly509del
XM_006714137.1:c.1744_1749del (F11)	XP_006714200.1:p.Glu582_Gly583del
XM_005262821.4:c.1792_1797del (F11)	XP_005262878.1:p.Glu598_Gly599del
XM_005262822.4:c.1696_1701del (F11)	XP_005262879.1:p.Glu566_Gly567del
XM_005262823.4:c.1522_1527del (F11)	XP_005262880.1:p.Glu508_Gly509del
XM_006714137.3:c.1744_1749del (F11)	XP_006714200.1:p.Glu582_Gly583del
NM_000128.4:c.1789_1794del (F11) MANE Select	NP_000119.1:p.Glu597_Gly598del