Canonical Allele Identifier: CA2740606789

Gene: F11 F11-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287832G>A , CM000666.2:g.186287832G>A	GRCh38
NC_000004.11:g.187208986G>A , CM000666.1:g.187208986G>A	GRCh37
NC_000004.10:g.187445980G>A	NCBI36
NG_008051.1:g.26869G>A , LRG_583:g.26869G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1716+9G>A (F11) MANE Select	ENSP00000384957.2:n.1716+9G>A
ENST00000264691.4:c.316+9G>A (F11)
ENST00000264692.8:c.1554+9G>A (F11)	ENSP00000264692.5:n.1554+9G>A
ENST00000403665.6:c.1716+9G>A (F11)	ENSP00000384957.2:n.1716+9G>A
ENST00000503841.1:n.235+9G>A (F11)
NM_000128.3:c.1716+9G>A , LRG_583t1:c.1716+9G>A (F11)	NP_000119.1:n.1716+9G>A
NR_033900.1:n.1066+596C>T (F11-AS1)
XM_005262821.2:c.1719+9G>A (F11)	XP_005262878.1:n.1719+9G>A
XM_005262822.2:c.1623+9G>A (F11)	XP_005262879.1:n.1623+9G>A
XM_005262823.2:c.1449+9G>A (F11)	XP_005262880.1:n.1449+9G>A
XM_006714137.1:c.1671+9G>A (F11)	XP_006714200.1:n.1671+9G>A
XM_005262821.4:c.1719+9G>A (F11)	XP_005262878.1:n.1719+9G>A
XM_005262822.4:c.1623+9G>A (F11)	XP_005262879.1:n.1623+9G>A
XM_005262823.4:c.1449+9G>A (F11)	XP_005262880.1:n.1449+9G>A
XM_006714137.3:c.1671+9G>A (F11)	XP_006714200.1:n.1671+9G>A
NM_000128.4:c.1716+9G>A (F11) MANE Select	NP_000119.1:n.1716+9G>A