Canonical Allele Identifier: CA358945940

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187209640A>T (hg19) ; chr4:g.186288486A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288486A>T , CM000666.2:g.186288486A>T	GRCh38
NC_000004.11:g.187209640A>T , CM000666.1:g.187209640A>T	GRCh37
NC_000004.10:g.187446634A>T	NCBI36
NG_008051.1:g.27523A>T , LRG_583:g.27523A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1750A>T (F11) MANE Select	ENSP00000384957.2:p.Asn584Tyr
ENST00000264691.4:c.350A>T (F11)
ENST00000264692.8:c.1588A>T (F11)	ENSP00000264692.5:p.Asn530Tyr
ENST00000403665.6:c.1750A>T (F11)	ENSP00000384957.2:p.Asn584Tyr
ENST00000503841.1:n.269A>T (F11)
NM_000128.3:c.1750A>T , LRG_583t1:c.1750A>T (F11)	NP_000119.1:p.Asn584Tyr
NR_033900.1:n.1008T>A (F11-AS1)
XM_005262821.2:c.1753A>T (F11)	XP_005262878.1:p.Asn585Tyr
XM_005262822.2:c.1657A>T (F11)	XP_005262879.1:p.Asn553Tyr
XM_005262823.2:c.1483A>T (F11)	XP_005262880.1:p.Asn495Tyr
XM_006714137.1:c.1705A>T (F11)	XP_006714200.1:p.Asn569Tyr
XM_005262821.4:c.1753A>T (F11)	XP_005262878.1:p.Asn585Tyr
XM_005262822.4:c.1657A>T (F11)	XP_005262879.1:p.Asn553Tyr
XM_005262823.4:c.1483A>T (F11)	XP_005262880.1:p.Asn495Tyr
XM_006714137.3:c.1705A>T (F11)	XP_006714200.1:p.Asn569Tyr
NM_000128.4:c.1750A>T (F11) MANE Select	NP_000119.1:p.Asn584Tyr