Canonical Allele Identifier: CA2708194086

Gene: F11 F11-AS1

Linked Data

• dbSNP Id: rs2126790154

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288230del , CM000666.2:g.186288230del	GRCh38
NC_000004.11:g.187209384del , CM000666.1:g.187209384del	GRCh37
NC_000004.10:g.187446378del	NCBI36
NG_008051.1:g.27267del , LRG_583:g.27267del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1717-223del (F11) MANE Select	ENSP00000384957.2:n.1717-223del
ENST00000264691.4:c.317-223del (F11)
ENST00000264692.8:c.1555-223del (F11)	ENSP00000264692.5:n.1555-223del
ENST00000403665.6:c.1717-223del (F11)	ENSP00000384957.2:n.1717-223del
ENST00000503841.1:n.236-223del (F11)
NM_000128.3:c.1717-223del , LRG_583t1:c.1717-223del (F11)	NP_000119.1:n.1717-223del
NR_033900.1:n.1066+202del (F11-AS1)
XM_005262821.2:c.1720-223del (F11)	XP_005262878.1:n.1720-223del
XM_005262822.2:c.1624-223del (F11)	XP_005262879.1:n.1624-223del
XM_005262823.2:c.1450-223del (F11)	XP_005262880.1:n.1450-223del
XM_006714137.1:c.1672-223del (F11)	XP_006714200.1:n.1672-223del
XM_005262821.4:c.1720-223del (F11)	XP_005262878.1:n.1720-223del
XM_005262822.4:c.1624-223del (F11)	XP_005262879.1:n.1624-223del
XM_005262823.4:c.1450-223del (F11)	XP_005262880.1:n.1450-223del
XM_006714137.3:c.1672-223del (F11)	XP_006714200.1:n.1672-223del
NM_000128.4:c.1717-223del (F11) MANE Select	NP_000119.1:n.1717-223del