Canonical Allele Identifier: CA358945667

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187208937T>C (hg19) ; chr4:g.186287783T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287783T>C , CM000666.2:g.186287783T>C	GRCh38
NC_000004.11:g.187208937T>C , CM000666.1:g.187208937T>C	GRCh37
NC_000004.10:g.187445931T>C	NCBI36
NG_008051.1:g.26820T>C , LRG_583:g.26820T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1676T>C (F11) MANE Select	ENSP00000384957.2:p.Ile559Thr
ENST00000264691.4:c.276T>C (F11)
ENST00000264692.8:c.1514T>C (F11)	ENSP00000264692.5:p.Ile505Thr
ENST00000403665.6:c.1676T>C (F11)	ENSP00000384957.2:p.Ile559Thr
ENST00000503841.1:n.195T>C (F11)
NM_000128.3:c.1676T>C , LRG_583t1:c.1676T>C (F11)	NP_000119.1:p.Ile559Thr
NR_033900.1:n.1066+645A>G (F11-AS1)
XM_005262821.2:c.1679T>C (F11)	XP_005262878.1:p.Ile560Thr
XM_005262822.2:c.1583T>C (F11)	XP_005262879.1:p.Ile528Thr
XM_005262823.2:c.1409T>C (F11)	XP_005262880.1:p.Ile470Thr
XM_006714137.1:c.1631T>C (F11)	XP_006714200.1:p.Ile544Thr
XM_005262821.4:c.1679T>C (F11)	XP_005262878.1:p.Ile560Thr
XM_005262822.4:c.1583T>C (F11)	XP_005262879.1:p.Ile528Thr
XM_005262823.4:c.1409T>C (F11)	XP_005262880.1:p.Ile470Thr
XM_006714137.3:c.1631T>C (F11)	XP_006714200.1:p.Ile544Thr
NM_000128.4:c.1676T>C (F11) MANE Select	NP_000119.1:p.Ile559Thr