Canonical Allele Identifier: CA358941532

Gene: F11

Linked Data

• dbSNP Id: rs1191394405
• MyVariant Identifiers: chr4:g.187205255C>T (hg19) ; chr4:g.186284101C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284101C>T , CM000666.2:g.186284101C>T	GRCh38
NC_000004.11:g.187205255C>T , CM000666.1:g.187205255C>T	GRCh37
NC_000004.10:g.187442249C>T	NCBI36
NG_008051.1:g.23138C>T , LRG_583:g.23138C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1145C>T MANE Select	ENSP00000384957.2:p.Thr382Ile
ENST00000264692.8:c.983C>T	ENSP00000264692.5:p.Thr328Ile
ENST00000403665.6:c.1145C>T	ENSP00000384957.2:p.Thr382Ile
NM_000128.3:c.1145C>T , LRG_583t1:c.1145C>T	NP_000119.1:p.Thr382Ile
XM_005262821.2:c.1148C>T	XP_005262878.1:p.Thr383Ile
XM_005262822.2:c.1148C>T	XP_005262879.1:p.Thr383Ile
XM_005262823.2:c.878C>T	XP_005262880.1:p.Thr293Ile
XM_005262824.1:c.1148C>T	XP_005262881.1:p.Thr383Ile
XM_006714137.1:c.1100C>T	XP_006714200.1:p.Thr367Ile
XR_938706.1:n.1553C>T
XR_938707.1:n.1553C>T
XM_005262821.4:c.1148C>T	XP_005262878.1:p.Thr383Ile
XM_005262822.4:c.1148C>T	XP_005262879.1:p.Thr383Ile
XM_005262823.4:c.878C>T	XP_005262880.1:p.Thr293Ile
XM_006714137.3:c.1100C>T	XP_006714200.1:p.Thr367Ile
XM_017007884.2:c.*2117C>T	XP_016863373.1:n.*2117C>T
XM_017007885.2:c.*13C>T	XP_016863374.1:n.*13C>T
XR_001741172.2:n.1619C>T
NM_000128.4:c.1145C>T MANE Select	NP_000119.1:p.Thr382Ile