Canonical Allele Identifier: CA358943309

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187206868T>A (hg19) ; chr4:g.186285714T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285714T>A , CM000666.2:g.186285714T>A	GRCh38
NC_000004.11:g.187206868T>A , CM000666.1:g.187206868T>A	GRCh37
NC_000004.10:g.187443862T>A	NCBI36
NG_008051.1:g.24751T>A , LRG_583:g.24751T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1381T>A MANE Select	ENSP00000384957.2:p.Phe461Ile
ENST00000264691.4:c.77T>A
ENST00000264692.8:c.1219T>A	ENSP00000264692.5:p.Phe407Ile
ENST00000403665.6:c.1381T>A	ENSP00000384957.2:p.Phe461Ile
NM_000128.3:c.1381T>A , LRG_583t1:c.1381T>A	NP_000119.1:p.Phe461Ile
XM_005262821.2:c.1384T>A	XP_005262878.1:p.Phe462Ile
XM_005262822.2:c.1384T>A	XP_005262879.1:p.Phe462Ile
XM_005262823.2:c.1114T>A	XP_005262880.1:p.Phe372Ile
XM_005262824.1:c.1384T>A	XP_005262881.1:p.Phe462Ile
XM_006714137.1:c.1336T>A	XP_006714200.1:p.Phe446Ile
XR_938706.1:n.1789T>A
XR_938707.1:n.1789T>A
XM_005262821.4:c.1384T>A	XP_005262878.1:p.Phe462Ile
XM_005262822.4:c.1384T>A	XP_005262879.1:p.Phe462Ile
XM_005262823.4:c.1114T>A	XP_005262880.1:p.Phe372Ile
XM_006714137.3:c.1336T>A	XP_006714200.1:p.Phe446Ile
XR_001741172.2:n.1855T>A
NM_000128.4:c.1381T>A MANE Select	NP_000119.1:p.Phe461Ile