Canonical Allele Identifier: CA358945678

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187208942G>A (hg19) ; chr4:g.186287788G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287788G>A , CM000666.2:g.186287788G>A	GRCh38
NC_000004.11:g.187208942G>A , CM000666.1:g.187208942G>A	GRCh37
NC_000004.10:g.187445936G>A	NCBI36
NG_008051.1:g.26825G>A , LRG_583:g.26825G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1681G>A (F11) MANE Select	ENSP00000384957.2:p.Ala561Thr
ENST00000264691.4:c.281G>A (F11)
ENST00000264692.8:c.1519G>A (F11)	ENSP00000264692.5:p.Ala507Thr
ENST00000403665.6:c.1681G>A (F11)	ENSP00000384957.2:p.Ala561Thr
ENST00000503841.1:n.200G>A (F11)
NM_000128.3:c.1681G>A , LRG_583t1:c.1681G>A (F11)	NP_000119.1:p.Ala561Thr
NR_033900.1:n.1066+640C>T (F11-AS1)
XM_005262821.2:c.1684G>A (F11)	XP_005262878.1:p.Ala562Thr
XM_005262822.2:c.1588G>A (F11)	XP_005262879.1:p.Ala530Thr
XM_005262823.2:c.1414G>A (F11)	XP_005262880.1:p.Ala472Thr
XM_006714137.1:c.1636G>A (F11)	XP_006714200.1:p.Ala546Thr
XM_005262821.4:c.1684G>A (F11)	XP_005262878.1:p.Ala562Thr
XM_005262822.4:c.1588G>A (F11)	XP_005262879.1:p.Ala530Thr
XM_005262823.4:c.1414G>A (F11)	XP_005262880.1:p.Ala472Thr
XM_006714137.3:c.1636G>A (F11)	XP_006714200.1:p.Ala546Thr
NM_000128.4:c.1681G>A (F11) MANE Select	NP_000119.1:p.Ala561Thr