Canonical Allele Identifier: CA1519939429

Gene: F11 F11-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287762A= , CM000666.2:g.186287762A=	GRCh38
NC_000004.11:g.187208916A= , CM000666.1:g.187208916A=	GRCh37
NC_000004.10:g.187445910A=	NCBI36
NG_008051.1:g.26799A= , LRG_583:g.26799A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1655A= (F11) MANE Select	ENSP00000384957.2:p.His552=
ENST00000264691.4:c.255A= (F11)
ENST00000264692.8:c.1493A= (F11)	ENSP00000264692.5:p.His498=
ENST00000403665.6:c.1655A= (F11)	ENSP00000384957.2:p.His552=
ENST00000503841.1:n.174A= (F11)
NM_000128.3:c.1655A= , LRG_583t1:c.1655A= (F11)	NP_000119.1:p.His552=
NR_033900.1:n.1066+666T= (F11-AS1)
XM_005262821.2:c.1658A= (F11)	XP_005262878.1:p.His553=
XM_005262822.2:c.1562A= (F11)	XP_005262879.1:p.His521=
XM_005262823.2:c.1388A= (F11)	XP_005262880.1:p.His463=
XM_006714137.1:c.1610A= (F11)	XP_006714200.1:p.His537=
XR_938707.1:n.1967A= (F11)
XM_005262821.4:c.1658A= (F11)	XP_005262878.1:p.His553=
XM_005262822.4:c.1562A= (F11)	XP_005262879.1:p.His521=
XM_005262823.4:c.1388A= (F11)	XP_005262880.1:p.His463=
XM_006714137.3:c.1610A= (F11)	XP_006714200.1:p.His537=
NM_000128.4:c.1655A= (F11) MANE Select	NP_000119.1:p.His552=