Canonical Allele Identifier: CA442641099

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187208845A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287691A>C , CM000666.2:g.186287691A>C	GRCh38
NC_000004.11:g.187208845A>C , CM000666.1:g.187208845A>C	GRCh37
NC_000004.10:g.187445839A>C	NCBI36
NG_008051.1:g.26728A>C , LRG_583:g.26728A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1584A>C (F11) MANE Select	ENSP00000384957.2:p.Ile528=
ENST00000264691.4:c.184A>C (F11)
ENST00000264692.8:c.1422A>C (F11)	ENSP00000264692.5:p.Ile474=
ENST00000403665.6:c.1584A>C (F11)	ENSP00000384957.2:p.Ile528=
ENST00000503841.1:n.103A>C (F11)
NM_000128.3:c.1584A>C , LRG_583t1:c.1584A>C (F11)	NP_000119.1:p.Ile528=
NR_033900.1:n.1066+737T>G (F11-AS1)
XM_005262821.2:c.1587A>C (F11)	XP_005262878.1:p.Ile529=
XM_005262822.2:c.1491A>C (F11)	XP_005262879.1:p.Ile497=
XM_005262823.2:c.1317A>C (F11)	XP_005262880.1:p.Ile439=
XM_006714137.1:c.1539A>C (F11)	XP_006714200.1:p.Ile513=
XR_938706.1:n.1992A>C (F11)
XR_938707.1:n.1896A>C (F11)
XM_005262821.4:c.1587A>C (F11)	XP_005262878.1:p.Ile529=
XM_005262822.4:c.1491A>C (F11)	XP_005262879.1:p.Ile497=
XM_005262823.4:c.1317A>C (F11)	XP_005262880.1:p.Ile439=
XM_006714137.3:c.1539A>C (F11)	XP_006714200.1:p.Ile513=
NM_000128.4:c.1584A>C (F11) MANE Select	NP_000119.1:p.Ile528=