Canonical Allele Identifier: CA2708194095

Gene: F11 F11-AS1

Linked Data

• dbSNP Id: rs2126790535

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288338_186288342del , CM000666.2:g.186288338_186288342del	GRCh38
NC_000004.11:g.187209492_187209496del , CM000666.1:g.187209492_187209496del	GRCh37
NC_000004.10:g.187446486_187446490del	NCBI36
NG_008051.1:g.27375_27379del , LRG_583:g.27375_27379del

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1717-115_1717-111del (F11) MANE Select	ENSP00000384957.2:n.1717-115_1717-111del
ENST00000264691.4:c.317-115_317-111del (F11)
ENST00000264692.8:c.1555-115_1555-111del (F11)	ENSP00000264692.5:n.1555-115_1555-111del
ENST00000403665.6:c.1717-115_1717-111del (F11)	ENSP00000384957.2:n.1717-115_1717-111del
ENST00000503841.1:n.236-115_236-111del (F11)
NM_000128.3:c.1717-115_1717-111del , LRG_583t1:c.1717-115_1717-111del (F11)	NP_000119.1:n.1717-115_1717-111del
NR_033900.1:n.1066+87_1066+91del (F11-AS1)
XM_005262821.2:c.1720-115_1720-111del (F11)	XP_005262878.1:n.1720-115_1720-111del
XM_005262822.2:c.1624-115_1624-111del (F11)	XP_005262879.1:n.1624-115_1624-111del
XM_005262823.2:c.1450-115_1450-111del (F11)	XP_005262880.1:n.1450-115_1450-111del
XM_006714137.1:c.1672-115_1672-111del (F11)	XP_006714200.1:n.1672-115_1672-111del
XM_005262821.4:c.1720-115_1720-111del (F11)	XP_005262878.1:n.1720-115_1720-111del
XM_005262822.4:c.1624-115_1624-111del (F11)	XP_005262879.1:n.1624-115_1624-111del
XM_005262823.4:c.1450-115_1450-111del (F11)	XP_005262880.1:n.1450-115_1450-111del
XM_006714137.3:c.1672-115_1672-111del (F11)	XP_006714200.1:n.1672-115_1672-111del
NM_000128.4:c.1717-115_1717-111del (F11) MANE Select	NP_000119.1:n.1717-115_1717-111del