Canonical Allele Identifier: CA358946118

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187209680A>T (hg19) ; chr4:g.186288526A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288526A>T , CM000666.2:g.186288526A>T	GRCh38
NC_000004.11:g.187209680A>T , CM000666.1:g.187209680A>T	GRCh37
NC_000004.10:g.187446674A>T	NCBI36
NG_008051.1:g.27563A>T , LRG_583:g.27563A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1790A>T (F11) MANE Select	ENSP00000384957.2:p.Glu597Val
ENST00000264691.4:c.390A>T (F11)
ENST00000264692.8:c.1628A>T (F11)	ENSP00000264692.5:p.Glu543Val
ENST00000403665.6:c.1790A>T (F11)	ENSP00000384957.2:p.Glu597Val
ENST00000503841.1:n.309A>T (F11)
NM_000128.3:c.1790A>T , LRG_583t1:c.1790A>T (F11)	NP_000119.1:p.Glu597Val
NR_033900.1:n.968T>A (F11-AS1)
XM_005262821.2:c.1793A>T (F11)	XP_005262878.1:p.Glu598Val
XM_005262822.2:c.1697A>T (F11)	XP_005262879.1:p.Glu566Val
XM_005262823.2:c.1523A>T (F11)	XP_005262880.1:p.Glu508Val
XM_006714137.1:c.1745A>T (F11)	XP_006714200.1:p.Glu582Val
XM_005262821.4:c.1793A>T (F11)	XP_005262878.1:p.Glu598Val
XM_005262822.4:c.1697A>T (F11)	XP_005262879.1:p.Glu566Val
XM_005262823.4:c.1523A>T (F11)	XP_005262880.1:p.Glu508Val
XM_006714137.3:c.1745A>T (F11)	XP_006714200.1:p.Glu582Val
NM_000128.4:c.1790A>T (F11) MANE Select	NP_000119.1:p.Glu597Val