Canonical Allele Identifier: CA358943678

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187206944T>G (hg19) ; chr4:g.186285790T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285790T>G , CM000666.2:g.186285790T>G	GRCh38
NC_000004.11:g.187206944T>G , CM000666.1:g.187206944T>G	GRCh37
NC_000004.10:g.187443938T>G	NCBI36
NG_008051.1:g.24827T>G , LRG_583:g.24827T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1457T>G MANE Select	ENSP00000384957.2:p.Leu486Arg
ENST00000264691.4:c.153T>G
ENST00000264692.8:c.1295T>G	ENSP00000264692.5:p.Leu432Arg
ENST00000403665.6:c.1457T>G	ENSP00000384957.2:p.Leu486Arg
NM_000128.3:c.1457T>G , LRG_583t1:c.1457T>G	NP_000119.1:p.Leu486Arg
XM_005262821.2:c.1460T>G	XP_005262878.1:p.Leu487Arg
XM_005262822.2:c.1460T>G	XP_005262879.1:p.Leu487Arg
XM_005262823.2:c.1190T>G	XP_005262880.1:p.Leu397Arg
XM_005262824.1:c.1460T>G	XP_005262881.1:p.Leu487Arg
XM_006714137.1:c.1412T>G	XP_006714200.1:p.Leu471Arg
XR_938706.1:n.1865T>G
XR_938707.1:n.1865T>G
XM_005262821.4:c.1460T>G	XP_005262878.1:p.Leu487Arg
XM_005262822.4:c.1460T>G	XP_005262879.1:p.Leu487Arg
XM_005262823.4:c.1190T>G	XP_005262880.1:p.Leu397Arg
XM_006714137.3:c.1412T>G	XP_006714200.1:p.Leu471Arg
XR_001741172.2:n.1931T>G
NM_000128.4:c.1457T>G MANE Select	NP_000119.1:p.Leu486Arg