Canonical Allele Identifier: CA358944398

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187207663A>T (hg19) ; chr4:g.186286509A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186286509A>T , CM000666.2:g.186286509A>T	GRCh38
NC_000004.11:g.187207663A>T , CM000666.1:g.187207663A>T	GRCh37
NC_000004.10:g.187444657A>T	NCBI36
NG_008051.1:g.25546A>T , LRG_583:g.25546A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1575A>T (F11) MANE Select	ENSP00000384957.2:p.Arg525Ser
ENST00000264691.4:c.176+696A>T (F11)
ENST00000264692.8:c.1413A>T (F11)	ENSP00000264692.5:p.Arg471Ser
ENST00000403665.6:c.1575A>T (F11)	ENSP00000384957.2:p.Arg525Ser
NM_000128.3:c.1575A>T , LRG_583t1:c.1575A>T (F11)	NP_000119.1:p.Arg525Ser
NR_033900.1:n.1067-243T>A (F11-AS1)
XM_005262821.2:c.1578A>T (F11)	XP_005262878.1:p.Arg526Ser
XM_005262822.2:c.1483+696A>T (F11)	XP_005262879.1:n.1483+696A>T
XM_005262823.2:c.1308A>T (F11)	XP_005262880.1:p.Arg436Ser
XM_005262824.1:c.1484-37A>T (F11)	XP_005262881.1:n.1484-37A>T
XM_006714137.1:c.1530A>T (F11)	XP_006714200.1:p.Arg510Ser
XR_938706.1:n.1983A>T (F11)
XR_938707.1:n.1888+696A>T (F11)
XM_005262821.4:c.1578A>T (F11)	XP_005262878.1:p.Arg526Ser
XM_005262822.4:c.1483+696A>T (F11)	XP_005262879.1:n.1483+696A>T
XM_005262823.4:c.1308A>T (F11)	XP_005262880.1:p.Arg436Ser
XM_006714137.3:c.1530A>T (F11)	XP_006714200.1:p.Arg510Ser
NM_000128.4:c.1575A>T (F11) MANE Select	NP_000119.1:p.Arg525Ser