Canonical Allele Identifier: CA3163738
Gene: F11 HGNC NCBI

Linked Data

dbSNP Id: rs768218948

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186276278A>T , CM000666.2:g.186276278A>T GRCh38
NC_000004.11:g.187197432A>T , CM000666.1:g.187197432A>T GRCh37
NC_000004.10:g.187434426A>T NCBI36
NG_008051.1:g.15315A>T , LRG_583:g.15315A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.643A>T MANE Select ENSP00000384957.2:p.Ile215Phe
ENST00000264692.8:c.481A>T ENSP00000264692.5:p.Ile161Phe
ENST00000403665.6:c.643A>T ENSP00000384957.2:p.Ile215Phe
ENST00000452239.1:c.90A>T
NM_000128.3:c.643A>T , LRG_583t1:c.643A>T NP_000119.1:p.Ile215Phe
XM_005262821.2:c.643A>T XP_005262878.1:p.Ile215Phe
XM_005262822.2:c.643A>T XP_005262879.1:p.Ile215Phe
XM_005262823.2:c.485+2003A>T XP_005262880.1:n.485+2003A>T
XM_005262824.1:c.643A>T XP_005262881.1:p.Ile215Phe
XM_006714137.1:c.643A>T XP_006714200.1:p.Ile215Phe
XR_938706.1:n.995A>T
XR_938707.1:n.995A>T
XM_005262821.4:c.643A>T XP_005262878.1:p.Ile215Phe
XM_005262822.4:c.643A>T XP_005262879.1:p.Ile215Phe
XM_005262823.4:c.485+2003A>T XP_005262880.1:n.485+2003A>T
XM_006714137.3:c.643A>T XP_006714200.1:p.Ile215Phe
XM_017007884.2:c.643A>T XP_016863373.1:p.Ile215Phe
XM_017007885.2:c.643A>T XP_016863374.1:p.Ile215Phe
XM_017007886.2:c.643A>T XP_016863375.1:p.Ile215Phe
XR_001741172.2:n.976A>T
NM_000128.4:c.643A>T MANE Select NP_000119.1:p.Ile215Phe