Canonical Allele Identifier: CA358941912

Gene: F11

Linked Data

• gnomAD v4: 4-186284176-C-G
• MyVariant Identifiers: chr4:g.187205330C>G (hg19) ; chr4:g.186284176C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284176C>G , CM000666.2:g.186284176C>G	GRCh38
NC_000004.11:g.187205330C>G , CM000666.1:g.187205330C>G	GRCh37
NC_000004.10:g.187442324C>G	NCBI36
NG_008051.1:g.23213C>G , LRG_583:g.23213C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1220C>G MANE Select	ENSP00000384957.2:p.Thr407Arg
ENST00000264692.8:c.1058C>G	ENSP00000264692.5:p.Thr353Arg
ENST00000403665.6:c.1220C>G	ENSP00000384957.2:p.Thr407Arg
NM_000128.3:c.1220C>G , LRG_583t1:c.1220C>G	NP_000119.1:p.Thr407Arg
XM_005262821.2:c.1223C>G	XP_005262878.1:p.Thr408Arg
XM_005262822.2:c.1223C>G	XP_005262879.1:p.Thr408Arg
XM_005262823.2:c.953C>G	XP_005262880.1:p.Thr318Arg
XM_005262824.1:c.1223C>G	XP_005262881.1:p.Thr408Arg
XM_006714137.1:c.1175C>G	XP_006714200.1:p.Thr392Arg
XR_938706.1:n.1628C>G
XR_938707.1:n.1628C>G
XM_005262821.4:c.1223C>G	XP_005262878.1:p.Thr408Arg
XM_005262822.4:c.1223C>G	XP_005262879.1:p.Thr408Arg
XM_005262823.4:c.953C>G	XP_005262880.1:p.Thr318Arg
XM_006714137.3:c.1175C>G	XP_006714200.1:p.Thr392Arg
XM_017007884.2:c.*2192C>G	XP_016863373.1:n.*2192C>G
XR_001741172.2:n.1694C>G
NM_000128.4:c.1220C>G MANE Select	NP_000119.1:p.Thr407Arg