Canonical Allele Identifier: CA358959083

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187197417T>G (hg19) ; chr4:g.186276263T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186276263T>G , CM000666.2:g.186276263T>G	GRCh38
NC_000004.11:g.187197417T>G , CM000666.1:g.187197417T>G	GRCh37
NC_000004.10:g.187434411T>G	NCBI36
NG_008051.1:g.15300T>G , LRG_583:g.15300T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.628T>G MANE Select	ENSP00000384957.2:p.Phe210Val
ENST00000264692.8:c.466T>G	ENSP00000264692.5:p.Phe156Val
ENST00000403665.6:c.628T>G	ENSP00000384957.2:p.Phe210Val
ENST00000452239.1:c.75T>G
NM_000128.3:c.628T>G , LRG_583t1:c.628T>G	NP_000119.1:p.Phe210Val
XM_005262821.2:c.628T>G	XP_005262878.1:p.Phe210Val
XM_005262822.2:c.628T>G	XP_005262879.1:p.Phe210Val
XM_005262823.2:c.485+1988T>G	XP_005262880.1:n.485+1988T>G
XM_005262824.1:c.628T>G	XP_005262881.1:p.Phe210Val
XM_006714137.1:c.628T>G	XP_006714200.1:p.Phe210Val
XR_938706.1:n.980T>G
XR_938707.1:n.980T>G
XM_005262821.4:c.628T>G	XP_005262878.1:p.Phe210Val
XM_005262822.4:c.628T>G	XP_005262879.1:p.Phe210Val
XM_005262823.4:c.485+1988T>G	XP_005262880.1:n.485+1988T>G
XM_006714137.3:c.628T>G	XP_006714200.1:p.Phe210Val
XM_017007884.2:c.628T>G	XP_016863373.1:p.Phe210Val
XM_017007885.2:c.628T>G	XP_016863374.1:p.Phe210Val
XM_017007886.2:c.628T>G	XP_016863375.1:p.Phe210Val
XR_001741172.2:n.961T>G
NM_000128.4:c.628T>G MANE Select	NP_000119.1:p.Phe210Val