Canonical Allele Identifier: CA358941518

Gene: F11

Linked Data

• dbSNP Id: rs1740995148
• MyVariant Identifiers: chr4:g.187205252C>T (hg19) ; chr4:g.186284098C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284098C>T , CM000666.2:g.186284098C>T	GRCh38
NC_000004.11:g.187205252C>T , CM000666.1:g.187205252C>T	GRCh37
NC_000004.10:g.187442246C>T	NCBI36
NG_008051.1:g.23135C>T , LRG_583:g.23135C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1142C>T MANE Select	ENSP00000384957.2:p.Thr381Ile
ENST00000264692.8:c.980C>T	ENSP00000264692.5:p.Thr327Ile
ENST00000403665.6:c.1142C>T	ENSP00000384957.2:p.Thr381Ile
NM_000128.3:c.1142C>T , LRG_583t1:c.1142C>T	NP_000119.1:p.Thr381Ile
XM_005262821.2:c.1145C>T	XP_005262878.1:p.Thr382Ile
XM_005262822.2:c.1145C>T	XP_005262879.1:p.Thr382Ile
XM_005262823.2:c.875C>T	XP_005262880.1:p.Thr292Ile
XM_005262824.1:c.1145C>T	XP_005262881.1:p.Thr382Ile
XM_006714137.1:c.1097C>T	XP_006714200.1:p.Thr366Ile
XR_938706.1:n.1550C>T
XR_938707.1:n.1550C>T
XM_005262821.4:c.1145C>T	XP_005262878.1:p.Thr382Ile
XM_005262822.4:c.1145C>T	XP_005262879.1:p.Thr382Ile
XM_005262823.4:c.875C>T	XP_005262880.1:p.Thr292Ile
XM_006714137.3:c.1097C>T	XP_006714200.1:p.Thr366Ile
XM_017007884.2:c.*2114C>T	XP_016863373.1:n.*2114C>T
XM_017007885.2:c.*10C>T	XP_016863374.1:n.*10C>T
XR_001741172.2:n.1616C>T
NM_000128.4:c.1142C>T MANE Select	NP_000119.1:p.Thr381Ile