Canonical Allele Identifier: CA358945460

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186287690T>G , CM000666.2:g.186287690T>G GRCh38
NC_000004.11:g.187208844T>G , CM000666.1:g.187208844T>G GRCh37
NC_000004.10:g.187445838T>G NCBI36
NG_008051.1:g.26727T>G , LRG_583:g.26727T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1583T>G (F11) MANE Select ENSP00000384957.2:p.Ile528Arg
ENST00000264691.4:c.183T>G (F11)
ENST00000264692.8:c.1421T>G (F11) ENSP00000264692.5:p.Ile474Arg
ENST00000403665.6:c.1583T>G (F11) ENSP00000384957.2:p.Ile528Arg
ENST00000503841.1:n.102T>G (F11)
NM_000128.3:c.1583T>G , LRG_583t1:c.1583T>G (F11) NP_000119.1:p.Ile528Arg
NR_033900.1:n.1066+738A>C (F11-AS1)
XM_005262821.2:c.1586T>G (F11) XP_005262878.1:p.Ile529Arg
XM_005262822.2:c.1490T>G (F11) XP_005262879.1:p.Ile497Arg
XM_005262823.2:c.1316T>G (F11) XP_005262880.1:p.Ile439Arg
XM_006714137.1:c.1538T>G (F11) XP_006714200.1:p.Ile513Arg
XR_938706.1:n.1991T>G (F11)
XR_938707.1:n.1895T>G (F11)
XM_005262821.4:c.1586T>G (F11) XP_005262878.1:p.Ile529Arg
XM_005262822.4:c.1490T>G (F11) XP_005262879.1:p.Ile497Arg
XM_005262823.4:c.1316T>G (F11) XP_005262880.1:p.Ile439Arg
XM_006714137.3:c.1538T>G (F11) XP_006714200.1:p.Ile513Arg
NM_000128.4:c.1583T>G (F11) MANE Select NP_000119.1:p.Ile528Arg