Canonical Allele Identifier: CA1519934175
Gene: F11 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.643A= MANE Select ENSP00000384957.2:p.Ile215=
ENST00000264692.8:c.481A= ENSP00000264692.5:p.Ile161=
ENST00000403665.6:c.643A= ENSP00000384957.2:p.Ile215=
ENST00000452239.1:c.90A=
NM_000128.3:c.643A= , LRG_583t1:c.643A= NP_000119.1:p.Ile215=
XM_005262821.2:c.643A= XP_005262878.1:p.Ile215=
XM_005262822.2:c.643A= XP_005262879.1:p.Ile215=
XM_005262823.2:c.485+2003A= XP_005262880.1:n.485+2003A=
XM_005262824.1:c.643A= XP_005262881.1:p.Ile215=
XM_006714137.1:c.643A= XP_006714200.1:p.Ile215=
XR_938706.1:n.995A=
XR_938707.1:n.995A=
XM_005262821.4:c.643A= XP_005262878.1:p.Ile215=
XM_005262822.4:c.643A= XP_005262879.1:p.Ile215=
XM_005262823.4:c.485+2003A= XP_005262880.1:n.485+2003A=
XM_006714137.3:c.643A= XP_006714200.1:p.Ile215=
XM_017007884.2:c.643A= XP_016863373.1:p.Ile215=
XM_017007885.2:c.643A= XP_016863374.1:p.Ile215=
XM_017007886.2:c.643A= XP_016863375.1:p.Ile215=
XR_001741172.2:n.976A=
NM_000128.4:c.643A= MANE Select NP_000119.1:p.Ile215=