Canonical Allele Identifier: CA442641375

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187209669G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288515G>C , CM000666.2:g.186288515G>C	GRCh38
NC_000004.11:g.187209669G>C , CM000666.1:g.187209669G>C	GRCh37
NC_000004.10:g.187446663G>C	NCBI36
NG_008051.1:g.27552G>C , LRG_583:g.27552G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1779G>C (F11) MANE Select	ENSP00000384957.2:p.Thr593=
ENST00000264691.4:c.379G>C (F11)
ENST00000264692.8:c.1617G>C (F11)	ENSP00000264692.5:p.Thr539=
ENST00000403665.6:c.1779G>C (F11)	ENSP00000384957.2:p.Thr593=
ENST00000503841.1:n.298G>C (F11)
NM_000128.3:c.1779G>C , LRG_583t1:c.1779G>C (F11)	NP_000119.1:p.Thr593=
NR_033900.1:n.979C>G (F11-AS1)
XM_005262821.2:c.1782G>C (F11)	XP_005262878.1:p.Thr594=
XM_005262822.2:c.1686G>C (F11)	XP_005262879.1:p.Thr562=
XM_005262823.2:c.1512G>C (F11)	XP_005262880.1:p.Thr504=
XM_006714137.1:c.1734G>C (F11)	XP_006714200.1:p.Thr578=
XM_005262821.4:c.1782G>C (F11)	XP_005262878.1:p.Thr594=
XM_005262822.4:c.1686G>C (F11)	XP_005262879.1:p.Thr562=
XM_005262823.4:c.1512G>C (F11)	XP_005262880.1:p.Thr504=
XM_006714137.3:c.1734G>C (F11)	XP_006714200.1:p.Thr578=
NM_000128.4:c.1779G>C (F11) MANE Select	NP_000119.1:p.Thr593=