Canonical Allele Identifier: CA442641128

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187208890A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287736A>G , CM000666.2:g.186287736A>G	GRCh38
NC_000004.11:g.187208890A>G , CM000666.1:g.187208890A>G	GRCh37
NC_000004.10:g.187445884A>G	NCBI36
NG_008051.1:g.26773A>G , LRG_583:g.26773A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1629A>G (F11) MANE Select	ENSP00000384957.2:p.Glu543=
ENST00000264691.4:c.229A>G (F11)
ENST00000264692.8:c.1467A>G (F11)	ENSP00000264692.5:p.Glu489=
ENST00000403665.6:c.1629A>G (F11)	ENSP00000384957.2:p.Glu543=
ENST00000503841.1:n.148A>G (F11)
NM_000128.3:c.1629A>G , LRG_583t1:c.1629A>G (F11)	NP_000119.1:p.Glu543=
NR_033900.1:n.1066+692T>C (F11-AS1)
XM_005262821.2:c.1632A>G (F11)	XP_005262878.1:p.Glu544=
XM_005262822.2:c.1536A>G (F11)	XP_005262879.1:p.Glu512=
XM_005262823.2:c.1362A>G (F11)	XP_005262880.1:p.Glu454=
XM_006714137.1:c.1584A>G (F11)	XP_006714200.1:p.Glu528=
XR_938707.1:n.1941A>G (F11)
XM_005262821.4:c.1632A>G (F11)	XP_005262878.1:p.Glu544=
XM_005262822.4:c.1536A>G (F11)	XP_005262879.1:p.Glu512=
XM_005262823.4:c.1362A>G (F11)	XP_005262880.1:p.Glu454=
XM_006714137.3:c.1584A>G (F11)	XP_006714200.1:p.Glu528=
NM_000128.4:c.1629A>G (F11) MANE Select	NP_000119.1:p.Glu543=