Canonical Allele Identifier: CA1519939437

Gene: F11 F11-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287782_186287789delinsATCTGTGC , CM000666.2:g.186287782_186287789delinsATCTGTGC	GRCh38
NC_000004.11:g.187208936_187208943delinsATCTGTGC , CM000666.1:g.187208936_187208943delinsATCTGTGC	GRCh37
NC_000004.10:g.187445930_187445937delinsATCTGTGC	NCBI36
NG_008051.1:g.26819_26826delinsATCTGTGC , LRG_583:g.26819_26826delinsATCTGTGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1675_1682delinsATCTGTGC (F11) MANE Select	ENSP00000384957.2:p.Ile559=
ENST00000264691.4:c.275_282delinsATCTGTGC (F11)
ENST00000264692.8:c.1513_1520delinsATCTGTGC (F11)	ENSP00000264692.5:p.Ile505=
ENST00000403665.6:c.1675_1682delinsATCTGTGC (F11)	ENSP00000384957.2:p.Ile559=
ENST00000503841.1:n.194_201delinsATCTGTGC (F11)
NM_000128.3:c.1675_1682delinsATCTGTGC , LRG_583t1:c.1675_1682delinsATCTGTGC (F11)	NP_000119.1:p.Ile559=
NR_033900.1:n.1066+639_1066+646delinsGCACAGAT (F11-AS1)
XM_005262821.2:c.1678_1685delinsATCTGTGC (F11)	XP_005262878.1:p.Ile560=
XM_005262822.2:c.1582_1589delinsATCTGTGC (F11)	XP_005262879.1:p.Ile528=
XM_005262823.2:c.1408_1415delinsATCTGTGC (F11)	XP_005262880.1:p.Ile470=
XM_006714137.1:c.1630_1637delinsATCTGTGC (F11)	XP_006714200.1:p.Ile544=
XM_005262821.4:c.1678_1685delinsATCTGTGC (F11)	XP_005262878.1:p.Ile560=
XM_005262822.4:c.1582_1589delinsATCTGTGC (F11)	XP_005262879.1:p.Ile528=
XM_005262823.4:c.1408_1415delinsATCTGTGC (F11)	XP_005262880.1:p.Ile470=
XM_006714137.3:c.1630_1637delinsATCTGTGC (F11)	XP_006714200.1:p.Ile544=
NM_000128.4:c.1675_1682delinsATCTGTGC (F11) MANE Select	NP_000119.1:p.Ile559=