Canonical Allele Identifier: CA1519934066
Gene: F11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186276056C= , CM000666.2:g.186276056C= GRCh38
NC_000004.11:g.187197210C= , CM000666.1:g.187197210C= GRCh37
NC_000004.10:g.187434204C= NCBI36
NG_008051.1:g.15093C= , LRG_583:g.15093C=

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.595+160C= MANE Select ENSP00000384957.2:n.595+160C=
ENST00000264692.8:c.433+160C= ENSP00000264692.5:n.433+160C=
ENST00000403665.6:c.595+160C= ENSP00000384957.2:n.595+160C=
ENST00000452239.1:c.42+160C=
NM_000128.3:c.595+160C= , LRG_583t1:c.595+160C= NP_000119.1:n.595+160C=
XM_005262821.2:c.595+160C= XP_005262878.1:n.595+160C=
XM_005262822.2:c.595+160C= XP_005262879.1:n.595+160C=
XM_005262823.2:c.485+1781C= XP_005262880.1:n.485+1781C=
XM_005262824.1:c.595+160C= XP_005262881.1:n.595+160C=
XM_006714137.1:c.595+160C= XP_006714200.1:n.595+160C=
XR_938706.1:n.947+160C=
XR_938707.1:n.947+160C=
XM_005262821.4:c.595+160C= XP_005262878.1:n.595+160C=
XM_005262822.4:c.595+160C= XP_005262879.1:n.595+160C=
XM_005262823.4:c.485+1781C= XP_005262880.1:n.485+1781C=
XM_006714137.3:c.595+160C= XP_006714200.1:n.595+160C=
XM_017007884.2:c.595+160C= XP_016863373.1:n.595+160C=
XM_017007885.2:c.595+160C= XP_016863374.1:n.595+160C=
XM_017007886.2:c.595+160C= XP_016863375.1:n.595+160C=
XR_001741172.2:n.928+160C=
NM_000128.4:c.595+160C= MANE Select NP_000119.1:n.595+160C=