Canonical Allele Identifier: CA1519939449

Gene: F11 F11-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287810_186287811delinsAG , CM000666.2:g.186287810_186287811delinsAG	GRCh38
NC_000004.11:g.187208964_187208965delinsAG , CM000666.1:g.187208964_187208965delinsAG	GRCh37
NC_000004.10:g.187445958_187445959delinsAG	NCBI36
NG_008051.1:g.26847_26848delinsAG , LRG_583:g.26847_26848delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1703_1704delinsAG (F11) MANE Select	ENSP00000384957.2:p.Lys568=
ENST00000264691.4:c.303_304delinsAG (F11)
ENST00000264692.8:c.1541_1542delinsAG (F11)	ENSP00000264692.5:p.Lys514=
ENST00000403665.6:c.1703_1704delinsAG (F11)	ENSP00000384957.2:p.Lys568=
ENST00000503841.1:n.222_223delinsAG (F11)
NM_000128.3:c.1703_1704delinsAG , LRG_583t1:c.1703_1704delinsAG (F11)	NP_000119.1:p.Lys568=
NR_033900.1:n.1066+617_1066+618delinsCT (F11-AS1)
XM_005262821.2:c.1706_1707delinsAG (F11)	XP_005262878.1:p.Lys569=
XM_005262822.2:c.1610_1611delinsAG (F11)	XP_005262879.1:p.Lys537=
XM_005262823.2:c.1436_1437delinsAG (F11)	XP_005262880.1:p.Lys479=
XM_006714137.1:c.1658_1659delinsAG (F11)	XP_006714200.1:p.Lys553=
XM_005262821.4:c.1706_1707delinsAG (F11)	XP_005262878.1:p.Lys569=
XM_005262822.4:c.1610_1611delinsAG (F11)	XP_005262879.1:p.Lys537=
XM_005262823.4:c.1436_1437delinsAG (F11)	XP_005262880.1:p.Lys479=
XM_006714137.3:c.1658_1659delinsAG (F11)	XP_006714200.1:p.Lys553=
NM_000128.4:c.1703_1704delinsAG (F11) MANE Select	NP_000119.1:p.Lys568=