Canonical Allele Identifier: CA219170

Gene: F11

Linked Data

• ClinVar Variation Id: 68208
• ClinVar RCV Id: RCV000059041
• dbSNP Id: rs281875253
• MyVariant Identifiers: chr4:g.187201503C>T (hg19) ; chr4:g.186280349C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280349C>T , CM000666.2:g.186280349C>T	GRCh38
NC_000004.11:g.187201503C>T , CM000666.1:g.187201503C>T	GRCh37
NC_000004.10:g.187438497C>T	NCBI36
NG_008051.1:g.19386C>T , LRG_583:g.19386C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.992C>T MANE Select	ENSP00000384957.2:p.Thr331Ile
ENST00000264692.8:c.830C>T	ENSP00000264692.5:p.Thr277Ile
ENST00000403665.6:c.992C>T	ENSP00000384957.2:p.Thr331Ile
ENST00000452239.1:c.439C>T
NM_000128.3:c.992C>T , LRG_583t1:c.992C>T	NP_000119.1:p.Thr331Ile
XM_005262821.2:c.992C>T	XP_005262878.1:p.Thr331Ile
XM_005262822.2:c.992C>T	XP_005262879.1:p.Thr331Ile
XM_005262823.2:c.722C>T	XP_005262880.1:p.Thr241Ile
XM_005262824.1:c.992C>T	XP_005262881.1:p.Thr331Ile
XM_006714137.1:c.944C>T	XP_006714200.1:p.Thr315Ile
XR_938706.1:n.1344C>T
XR_938707.1:n.1344C>T
XM_005262821.4:c.992C>T	XP_005262878.1:p.Thr331Ile
XM_005262822.4:c.992C>T	XP_005262879.1:p.Thr331Ile
XM_005262823.4:c.722C>T	XP_005262880.1:p.Thr241Ile
XM_006714137.3:c.944C>T	XP_006714200.1:p.Thr315Ile
XM_017007884.2:c.992C>T	XP_016863373.1:p.Thr331Ile
XM_017007885.2:c.992C>T	XP_016863374.1:p.Thr331Ile
XM_017007886.2:c.992C>T	XP_016863375.1:p.Thr331Ile
XR_001741172.2:n.1325C>T
NM_000128.4:c.992C>T MANE Select	NP_000119.1:p.Thr331Ile