Canonical Allele Identifier: CA358959143
Gene: F11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186276288T>C , CM000666.2:g.186276288T>C GRCh38
NC_000004.11:g.187197442T>C , CM000666.1:g.187197442T>C GRCh37
NC_000004.10:g.187434436T>C NCBI36
NG_008051.1:g.15325T>C , LRG_583:g.15325T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.653T>C MANE Select ENSP00000384957.2:p.Val218Ala
ENST00000264692.8:c.491T>C ENSP00000264692.5:p.Val164Ala
ENST00000403665.6:c.653T>C ENSP00000384957.2:p.Val218Ala
ENST00000452239.1:c.100T>C
NM_000128.3:c.653T>C , LRG_583t1:c.653T>C NP_000119.1:p.Val218Ala
XM_005262821.2:c.653T>C XP_005262878.1:p.Val218Ala
XM_005262822.2:c.653T>C XP_005262879.1:p.Val218Ala
XM_005262823.2:c.485+2013T>C XP_005262880.1:n.485+2013T>C
XM_005262824.1:c.653T>C XP_005262881.1:p.Val218Ala
XM_006714137.1:c.653T>C XP_006714200.1:p.Val218Ala
XR_938706.1:n.1005T>C
XR_938707.1:n.1005T>C
XM_005262821.4:c.653T>C XP_005262878.1:p.Val218Ala
XM_005262822.4:c.653T>C XP_005262879.1:p.Val218Ala
XM_005262823.4:c.485+2013T>C XP_005262880.1:n.485+2013T>C
XM_006714137.3:c.653T>C XP_006714200.1:p.Val218Ala
XM_017007884.2:c.653T>C XP_016863373.1:p.Val218Ala
XM_017007885.2:c.653T>C XP_016863374.1:p.Val218Ala
XM_017007886.2:c.653T>C XP_016863375.1:p.Val218Ala
XR_001741172.2:n.986T>C
NM_000128.4:c.653T>C MANE Select NP_000119.1:p.Val218Ala