Canonical Allele Identifier: CA2764876921

Gene: F11 F11-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288426dup , CM000666.2:g.186288426dup	GRCh38
NC_000004.11:g.187209580dup , CM000666.1:g.187209580dup	GRCh37
NC_000004.10:g.187446574dup	NCBI36
NG_008051.1:g.27463dup , LRG_583:g.27463dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1717-27dup (F11) MANE Select	ENSP00000384957.2:n.1717-27dup
ENST00000264691.4:c.317-27dup (F11)
ENST00000264692.8:c.1555-27dup (F11)	ENSP00000264692.5:n.1555-27dup
ENST00000403665.6:c.1717-27dup (F11)	ENSP00000384957.2:n.1717-27dup
ENST00000503841.1:n.236-27dup (F11)
NM_000128.3:c.1717-27dup , LRG_583t1:c.1717-27dup (F11)	NP_000119.1:n.1717-27dup
NR_033900.1:n.1066+2dup (F11-AS1)
XM_005262821.2:c.1720-27dup (F11)	XP_005262878.1:n.1720-27dup
XM_005262822.2:c.1624-27dup (F11)	XP_005262879.1:n.1624-27dup
XM_005262823.2:c.1450-27dup (F11)	XP_005262880.1:n.1450-27dup
XM_006714137.1:c.1672-27dup (F11)	XP_006714200.1:n.1672-27dup
XM_005262821.4:c.1720-27dup (F11)	XP_005262878.1:n.1720-27dup
XM_005262822.4:c.1624-27dup (F11)	XP_005262879.1:n.1624-27dup
XM_005262823.4:c.1450-27dup (F11)	XP_005262880.1:n.1450-27dup
XM_006714137.3:c.1672-27dup (F11)	XP_006714200.1:n.1672-27dup
NM_000128.4:c.1717-27dup (F11) MANE Select	NP_000119.1:n.1717-27dup