Canonical Allele Identifier: CA358946040

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187209662G>T (hg19) ; chr4:g.186288508G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288508G>T , CM000666.2:g.186288508G>T	GRCh38
NC_000004.11:g.187209662G>T , CM000666.1:g.187209662G>T	GRCh37
NC_000004.10:g.187446656G>T	NCBI36
NG_008051.1:g.27545G>T , LRG_583:g.27545G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1772G>T (F11) MANE Select	ENSP00000384957.2:p.Gly591Val
ENST00000264691.4:c.372G>T (F11)
ENST00000264692.8:c.1610G>T (F11)	ENSP00000264692.5:p.Gly537Val
ENST00000403665.6:c.1772G>T (F11)	ENSP00000384957.2:p.Gly591Val
ENST00000503841.1:n.291G>T (F11)
NM_000128.3:c.1772G>T , LRG_583t1:c.1772G>T (F11)	NP_000119.1:p.Gly591Val
NR_033900.1:n.986C>A (F11-AS1)
XM_005262821.2:c.1775G>T (F11)	XP_005262878.1:p.Gly592Val
XM_005262822.2:c.1679G>T (F11)	XP_005262879.1:p.Gly560Val
XM_005262823.2:c.1505G>T (F11)	XP_005262880.1:p.Gly502Val
XM_006714137.1:c.1727G>T (F11)	XP_006714200.1:p.Gly576Val
XM_005262821.4:c.1775G>T (F11)	XP_005262878.1:p.Gly592Val
XM_005262822.4:c.1679G>T (F11)	XP_005262879.1:p.Gly560Val
XM_005262823.4:c.1505G>T (F11)	XP_005262880.1:p.Gly502Val
XM_006714137.3:c.1727G>T (F11)	XP_006714200.1:p.Gly576Val
NM_000128.4:c.1772G>T (F11) MANE Select	NP_000119.1:p.Gly591Val