Canonical Allele Identifier: CA2155133354
Gene: FBLN5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91870343T= , CM000676.2:g.91870343T= GRCh38
NC_000014.8:g.92336687T= , CM000676.1:g.92336687T= GRCh37
NC_000014.7:g.91406440T= NCBI36
NG_008254.1:g.82360A= , LRG_364:g.82360A=

Transcript Alleles

HGVS Amino-acid change
ENST00000557088.6:c.*1194A= ENSP00000451002.1:n.*1194A=
ENST00000557570.2:c.1060A= ENSP00000450787.2:p.Ile354=
ENST00000706675.1:n.1043A=
ENST00000706676.1:c.1402A= ENSP00000516492.1:p.Ile468=
ENST00000706677.1:c.*12A= ENSP00000516493.1:n.*12A=
ENST00000706678.1:n.1148A=
ENST00000706679.1:c.1060A= ENSP00000516494.1:p.Ile354=
ENST00000706680.1:c.*1071A= ENSP00000516495.1:n.*1071A=
ENST00000706681.1:c.*967A= ENSP00000516496.1:n.*967A=
ENST00000342058.9:c.1228A= MANE Select ENSP00000345008.4:p.Ile410=
ENST00000267620.14:c.1351A= ENSP00000267620.10:p.Ile451=
ENST00000342058.8:c.1228A= ENSP00000345008.4:p.Ile410=
ENST00000554121.2:n.354A=
ENST00000556154.5:c.1243A= ENSP00000451982.1:p.Ile415=
ENST00000556961.1:n.1363A=
NM_006329.3:c.1228A= , LRG_364t1:c.1228A= NP_006320.2:p.Ile410=
XM_005267267.3:c.1279A= XP_005267324.1:p.Ile427=
XM_011536356.1:c.*12A= XP_011534658.1:n.*12A=
XM_011536357.1:c.*12A= XP_011534659.1:n.*12A=
XM_011536358.1:c.*12A= XP_011534660.1:n.*12A=
XM_011536357.2:c.*12A= XP_011534659.1:n.*12A=
XM_011536358.2:c.*12A= XP_011534660.1:n.*12A=
XM_017020929.2:c.1060A= XP_016876418.1:p.Ile354=
NM_001384158.1:c.1351A= NP_001371087.1:p.Ile451=
NM_001384159.1:c.1279A= NP_001371088.1:p.Ile427=
NM_001384160.1:c.*12A= NP_001371089.1:n.*12A=
NM_001384161.1:c.*12A= NP_001371090.1:n.*12A=
NM_001384162.1:c.1060A= NP_001371091.1:p.Ile354=
NM_006329.4:c.1228A= MANE Select NP_006320.2:p.Ile410=