Canonical Allele Identifier: CA1519939711

Gene: F11 F11-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288262T= , CM000666.2:g.186288262T=	GRCh38
NC_000004.11:g.187209416T= , CM000666.1:g.187209416T=	GRCh37
NC_000004.10:g.187446410T=	NCBI36
NG_008051.1:g.27299T= , LRG_583:g.27299T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1717-191T= (F11) MANE Select	ENSP00000384957.2:n.1717-191T=
ENST00000264691.4:c.317-191T= (F11)
ENST00000264692.8:c.1555-191T= (F11)	ENSP00000264692.5:n.1555-191T=
ENST00000403665.6:c.1717-191T= (F11)	ENSP00000384957.2:n.1717-191T=
ENST00000503841.1:n.236-191T= (F11)
NM_000128.3:c.1717-191T= , LRG_583t1:c.1717-191T= (F11)	NP_000119.1:n.1717-191T=
NR_033900.1:n.1066+166A= (F11-AS1)
XM_005262821.2:c.1720-191T= (F11)	XP_005262878.1:n.1720-191T=
XM_005262822.2:c.1624-191T= (F11)	XP_005262879.1:n.1624-191T=
XM_005262823.2:c.1450-191T= (F11)	XP_005262880.1:n.1450-191T=
XM_006714137.1:c.1672-191T= (F11)	XP_006714200.1:n.1672-191T=
XM_005262821.4:c.1720-191T= (F11)	XP_005262878.1:n.1720-191T=
XM_005262822.4:c.1624-191T= (F11)	XP_005262879.1:n.1624-191T=
XM_005262823.4:c.1450-191T= (F11)	XP_005262880.1:n.1450-191T=
XM_006714137.3:c.1672-191T= (F11)	XP_006714200.1:n.1672-191T=
NM_000128.4:c.1717-191T= (F11) MANE Select	NP_000119.1:n.1717-191T=