Canonical Allele Identifier: CA442641109

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187208863A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287709A>G , CM000666.2:g.186287709A>G	GRCh38
NC_000004.11:g.187208863A>G , CM000666.1:g.187208863A>G	GRCh37
NC_000004.10:g.187445857A>G	NCBI36
NG_008051.1:g.26746A>G , LRG_583:g.26746A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1602A>G (F11) MANE Select	ENSP00000384957.2:p.Lys534=
ENST00000264691.4:c.202A>G (F11)
ENST00000264692.8:c.1440A>G (F11)	ENSP00000264692.5:p.Lys480=
ENST00000403665.6:c.1602A>G (F11)	ENSP00000384957.2:p.Lys534=
ENST00000503841.1:n.121A>G (F11)
NM_000128.3:c.1602A>G , LRG_583t1:c.1602A>G (F11)	NP_000119.1:p.Lys534=
NR_033900.1:n.1066+719T>C (F11-AS1)
XM_005262821.2:c.1605A>G (F11)	XP_005262878.1:p.Lys535=
XM_005262822.2:c.1509A>G (F11)	XP_005262879.1:p.Lys503=
XM_005262823.2:c.1335A>G (F11)	XP_005262880.1:p.Lys445=
XM_006714137.1:c.1557A>G (F11)	XP_006714200.1:p.Lys519=
XR_938707.1:n.1914A>G (F11)
XM_005262821.4:c.1605A>G (F11)	XP_005262878.1:p.Lys535=
XM_005262822.4:c.1509A>G (F11)	XP_005262879.1:p.Lys503=
XM_005262823.4:c.1335A>G (F11)	XP_005262880.1:p.Lys445=
XM_006714137.3:c.1557A>G (F11)	XP_006714200.1:p.Lys519=
NM_000128.4:c.1602A>G (F11) MANE Select	NP_000119.1:p.Lys534=