Canonical Allele Identifier: CA442641123

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187208884C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287730C>G , CM000666.2:g.186287730C>G	GRCh38
NC_000004.11:g.187208884C>G , CM000666.1:g.187208884C>G	GRCh37
NC_000004.10:g.187445878C>G	NCBI36
NG_008051.1:g.26767C>G , LRG_583:g.26767C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1623C>G (F11) MANE Select	ENSP00000384957.2:p.Thr541=
ENST00000264691.4:c.223C>G (F11)
ENST00000264692.8:c.1461C>G (F11)	ENSP00000264692.5:p.Thr487=
ENST00000403665.6:c.1623C>G (F11)	ENSP00000384957.2:p.Thr541=
ENST00000503841.1:n.142C>G (F11)
NM_000128.3:c.1623C>G , LRG_583t1:c.1623C>G (F11)	NP_000119.1:p.Thr541=
NR_033900.1:n.1066+698G>C (F11-AS1)
XM_005262821.2:c.1626C>G (F11)	XP_005262878.1:p.Thr542=
XM_005262822.2:c.1530C>G (F11)	XP_005262879.1:p.Thr510=
XM_005262823.2:c.1356C>G (F11)	XP_005262880.1:p.Thr452=
XM_006714137.1:c.1578C>G (F11)	XP_006714200.1:p.Thr526=
XR_938707.1:n.1935C>G (F11)
XM_005262821.4:c.1626C>G (F11)	XP_005262878.1:p.Thr542=
XM_005262822.4:c.1530C>G (F11)	XP_005262879.1:p.Thr510=
XM_005262823.4:c.1356C>G (F11)	XP_005262880.1:p.Thr452=
XM_006714137.3:c.1578C>G (F11)	XP_006714200.1:p.Thr526=
NM_000128.4:c.1623C>G (F11) MANE Select	NP_000119.1:p.Thr541=