Canonical Allele Identifier: CA1519938837

Gene: F11 F11-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186286487G= , CM000666.2:g.186286487G=	GRCh38
NC_000004.11:g.187207641G= , CM000666.1:g.187207641G=	GRCh37
NC_000004.10:g.187444635G=	NCBI36
NG_008051.1:g.25524G= , LRG_583:g.25524G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1553G= (F11) MANE Select	ENSP00000384957.2:p.Gly518=
ENST00000264691.4:c.176+674G= (F11)
ENST00000264692.8:c.1391G= (F11)	ENSP00000264692.5:p.Gly464=
ENST00000403665.6:c.1553G= (F11)	ENSP00000384957.2:p.Gly518=
NM_000128.3:c.1553G= , LRG_583t1:c.1553G= (F11)	NP_000119.1:p.Gly518=
NR_033900.1:n.1067-221C= (F11-AS1)
XM_005262821.2:c.1556G= (F11)	XP_005262878.1:p.Gly519=
XM_005262822.2:c.1483+674G= (F11)	XP_005262879.1:n.1483+674G=
XM_005262823.2:c.1286G= (F11)	XP_005262880.1:p.Gly429=
XM_005262824.1:c.1484-59G= (F11)	XP_005262881.1:n.1484-59G=
XM_006714137.1:c.1508G= (F11)	XP_006714200.1:p.Gly503=
XR_938706.1:n.1961G= (F11)
XR_938707.1:n.1888+674G= (F11)
XM_005262821.4:c.1556G= (F11)	XP_005262878.1:p.Gly519=
XM_005262822.4:c.1483+674G= (F11)	XP_005262879.1:n.1483+674G=
XM_005262823.4:c.1286G= (F11)	XP_005262880.1:p.Gly429=
XM_006714137.3:c.1508G= (F11)	XP_006714200.1:p.Gly503=
XR_001741172.2:n.2027G= (F11)
NM_000128.4:c.1553G= (F11) MANE Select	NP_000119.1:p.Gly518=