Canonical Allele Identifier: CA358946211

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187209703C>A (hg19) ; chr4:g.186288549C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288549C>A , CM000666.2:g.186288549C>A	GRCh38
NC_000004.11:g.187209703C>A , CM000666.1:g.187209703C>A	GRCh37
NC_000004.10:g.187446697C>A	NCBI36
NG_008051.1:g.27586C>A , LRG_583:g.27586C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1813C>A (F11) MANE Select	ENSP00000384957.2:p.Pro605Thr
ENST00000264691.4:c.413C>A (F11)
ENST00000264692.8:c.1651C>A (F11)	ENSP00000264692.5:p.Pro551Thr
ENST00000403665.6:c.1813C>A (F11)	ENSP00000384957.2:p.Pro605Thr
ENST00000503841.1:n.332C>A (F11)
NM_000128.3:c.1813C>A , LRG_583t1:c.1813C>A (F11)	NP_000119.1:p.Pro605Thr
NR_033900.1:n.945G>T (F11-AS1)
XM_005262821.2:c.1816C>A (F11)	XP_005262878.1:p.Pro606Thr
XM_005262822.2:c.1720C>A (F11)	XP_005262879.1:p.Pro574Thr
XM_005262823.2:c.1546C>A (F11)	XP_005262880.1:p.Pro516Thr
XM_006714137.1:c.1768C>A (F11)	XP_006714200.1:p.Pro590Thr
XM_005262821.4:c.1816C>A (F11)	XP_005262878.1:p.Pro606Thr
XM_005262822.4:c.1720C>A (F11)	XP_005262879.1:p.Pro574Thr
XM_005262823.4:c.1546C>A (F11)	XP_005262880.1:p.Pro516Thr
XM_006714137.3:c.1768C>A (F11)	XP_006714200.1:p.Pro590Thr
NM_000128.4:c.1813C>A (F11) MANE Select	NP_000119.1:p.Pro605Thr