Canonical Allele Identifier: CA442641368

Gene: F11 F11-AS1

Linked Data

• gnomAD v4: 4-186288506-A-G
• MyVariant Identifiers: chr4:g.187209660A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288506A>G , CM000666.2:g.186288506A>G	GRCh38
NC_000004.11:g.187209660A>G , CM000666.1:g.187209660A>G	GRCh37
NC_000004.10:g.187446654A>G	NCBI36
NG_008051.1:g.27543A>G , LRG_583:g.27543A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1770A>G (F11) MANE Select	ENSP00000384957.2:p.Val590=
ENST00000264691.4:c.370A>G (F11)
ENST00000264692.8:c.1608A>G (F11)	ENSP00000264692.5:p.Val536=
ENST00000403665.6:c.1770A>G (F11)	ENSP00000384957.2:p.Val590=
ENST00000503841.1:n.289A>G (F11)
NM_000128.3:c.1770A>G , LRG_583t1:c.1770A>G (F11)	NP_000119.1:p.Val590=
NR_033900.1:n.988T>C (F11-AS1)
XM_005262821.2:c.1773A>G (F11)	XP_005262878.1:p.Val591=
XM_005262822.2:c.1677A>G (F11)	XP_005262879.1:p.Val559=
XM_005262823.2:c.1503A>G (F11)	XP_005262880.1:p.Val501=
XM_006714137.1:c.1725A>G (F11)	XP_006714200.1:p.Val575=
XM_005262821.4:c.1773A>G (F11)	XP_005262878.1:p.Val591=
XM_005262822.4:c.1677A>G (F11)	XP_005262879.1:p.Val559=
XM_005262823.4:c.1503A>G (F11)	XP_005262880.1:p.Val501=
XM_006714137.3:c.1725A>G (F11)	XP_006714200.1:p.Val575=
NM_000128.4:c.1770A>G (F11) MANE Select	NP_000119.1:p.Val590=