Canonical Allele Identifier: CA358945462

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186287691A>G , CM000666.2:g.186287691A>G GRCh38
NC_000004.11:g.187208845A>G , CM000666.1:g.187208845A>G GRCh37
NC_000004.10:g.187445839A>G NCBI36
NG_008051.1:g.26728A>G , LRG_583:g.26728A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1584A>G (F11) MANE Select ENSP00000384957.2:p.Ile528Met
ENST00000264691.4:c.184A>G (F11)
ENST00000264692.8:c.1422A>G (F11) ENSP00000264692.5:p.Ile474Met
ENST00000403665.6:c.1584A>G (F11) ENSP00000384957.2:p.Ile528Met
ENST00000503841.1:n.103A>G (F11)
NM_000128.3:c.1584A>G , LRG_583t1:c.1584A>G (F11) NP_000119.1:p.Ile528Met
NR_033900.1:n.1066+737T>C (F11-AS1)
XM_005262821.2:c.1587A>G (F11) XP_005262878.1:p.Ile529Met
XM_005262822.2:c.1491A>G (F11) XP_005262879.1:p.Ile497Met
XM_005262823.2:c.1317A>G (F11) XP_005262880.1:p.Ile439Met
XM_006714137.1:c.1539A>G (F11) XP_006714200.1:p.Ile513Met
XR_938706.1:n.1992A>G (F11)
XR_938707.1:n.1896A>G (F11)
XM_005262821.4:c.1587A>G (F11) XP_005262878.1:p.Ile529Met
XM_005262822.4:c.1491A>G (F11) XP_005262879.1:p.Ile497Met
XM_005262823.4:c.1317A>G (F11) XP_005262880.1:p.Ile439Met
XM_006714137.3:c.1539A>G (F11) XP_006714200.1:p.Ile513Met
NM_000128.4:c.1584A>G (F11) MANE Select NP_000119.1:p.Ile528Met