Canonical Allele Identifier: CA358943191

Gene: F11

Linked Data

• gnomAD v4: 4-186285695-A-G
• COSMIC: COSM3131247 ; COSM4331365
• MyVariant Identifiers: chr4:g.187206849A>G (hg19) ; chr4:g.186285695A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285695A>G , CM000666.2:g.186285695A>G	GRCh38
NC_000004.11:g.187206849A>G , CM000666.1:g.187206849A>G	GRCh37
NC_000004.10:g.187443843A>G	NCBI36
NG_008051.1:g.24732A>G , LRG_583:g.24732A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1362A>G MANE Select	ENSP00000384957.2:p.Ile454Met
ENST00000264691.4:c.58A>G
ENST00000264692.8:c.1200A>G	ENSP00000264692.5:p.Ile400Met
ENST00000403665.6:c.1362A>G	ENSP00000384957.2:p.Ile454Met
NM_000128.3:c.1362A>G , LRG_583t1:c.1362A>G	NP_000119.1:p.Ile454Met
XM_005262821.2:c.1365A>G	XP_005262878.1:p.Ile455Met
XM_005262822.2:c.1365A>G	XP_005262879.1:p.Ile455Met
XM_005262823.2:c.1095A>G	XP_005262880.1:p.Ile365Met
XM_005262824.1:c.1365A>G	XP_005262881.1:p.Ile455Met
XM_006714137.1:c.1317A>G	XP_006714200.1:p.Ile439Met
XR_938706.1:n.1770A>G
XR_938707.1:n.1770A>G
XM_005262821.4:c.1365A>G	XP_005262878.1:p.Ile455Met
XM_005262822.4:c.1365A>G	XP_005262879.1:p.Ile455Met
XM_005262823.4:c.1095A>G	XP_005262880.1:p.Ile365Met
XM_006714137.3:c.1317A>G	XP_006714200.1:p.Ile439Met
XR_001741172.2:n.1836A>G
NM_000128.4:c.1362A>G MANE Select	NP_000119.1:p.Ile454Met