Canonical Allele Identifier: CA358946420

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187209766T>A (hg19) ; chr4:g.186288612T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288612T>A , CM000666.2:g.186288612T>A	GRCh38
NC_000004.11:g.187209766T>A , CM000666.1:g.187209766T>A	GRCh37
NC_000004.10:g.187446760T>A	NCBI36
NG_008051.1:g.27649T>A , LRG_583:g.27649T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1876T>A (F11) MANE Select	ENSP00000384957.2:p.Ter626Arg
ENST00000264691.4:c.476T>A (F11)
ENST00000264692.8:c.1714T>A (F11)	ENSP00000264692.5:p.Ter572Arg
ENST00000403665.6:c.1876T>A (F11)	ENSP00000384957.2:p.Ter626Arg
ENST00000503841.1:n.395T>A (F11)
NM_000128.3:c.1876T>A , LRG_583t1:c.1876T>A (F11)	NP_000119.1:p.Ter626Arg
NR_033900.1:n.882A>T (F11-AS1)
XM_005262821.2:c.1879T>A (F11)	XP_005262878.1:p.Ter627Arg
XM_005262822.2:c.1783T>A (F11)	XP_005262879.1:p.Ter595Arg
XM_005262823.2:c.1609T>A (F11)	XP_005262880.1:p.Ter537Arg
XM_006714137.1:c.1831T>A (F11)	XP_006714200.1:p.Ter611Arg
XM_005262821.4:c.1879T>A (F11)	XP_005262878.1:p.Ter627Arg
XM_005262822.4:c.1783T>A (F11)	XP_005262879.1:p.Ter595Arg
XM_005262823.4:c.1609T>A (F11)	XP_005262880.1:p.Ter537Arg
XM_006714137.3:c.1831T>A (F11)	XP_006714200.1:p.Ter611Arg
NM_000128.4:c.1876T>A (F11) MANE Select	NP_000119.1:p.Ter626Arg