Canonical Allele Identifier: CA442641104

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187208854T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287700T>C , CM000666.2:g.186287700T>C	GRCh38
NC_000004.11:g.187208854T>C , CM000666.1:g.187208854T>C	GRCh37
NC_000004.10:g.187445848T>C	NCBI36
NG_008051.1:g.26737T>C , LRG_583:g.26737T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1593T>C (F11) MANE Select	ENSP00000384957.2:p.Thr531=
ENST00000264691.4:c.193T>C (F11)
ENST00000264692.8:c.1431T>C (F11)	ENSP00000264692.5:p.Thr477=
ENST00000403665.6:c.1593T>C (F11)	ENSP00000384957.2:p.Thr531=
ENST00000503841.1:n.112T>C (F11)
NM_000128.3:c.1593T>C , LRG_583t1:c.1593T>C (F11)	NP_000119.1:p.Thr531=
NR_033900.1:n.1066+728A>G (F11-AS1)
XM_005262821.2:c.1596T>C (F11)	XP_005262878.1:p.Thr532=
XM_005262822.2:c.1500T>C (F11)	XP_005262879.1:p.Thr500=
XM_005262823.2:c.1326T>C (F11)	XP_005262880.1:p.Thr442=
XM_006714137.1:c.1548T>C (F11)	XP_006714200.1:p.Thr516=
XR_938706.1:n.2001T>C (F11)
XR_938707.1:n.1905T>C (F11)
XM_005262821.4:c.1596T>C (F11)	XP_005262878.1:p.Thr532=
XM_005262822.4:c.1500T>C (F11)	XP_005262879.1:p.Thr500=
XM_005262823.4:c.1326T>C (F11)	XP_005262880.1:p.Thr442=
XM_006714137.3:c.1548T>C (F11)	XP_006714200.1:p.Thr516=
NM_000128.4:c.1593T>C (F11) MANE Select	NP_000119.1:p.Thr531=