Canonical Allele Identifier: CA213144
Gene: FBLN5 HGNC NCBI

Linked Data

ClinVar Variation Id: 5481
dbSNP Id: rs28939073

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91877621G>A , CM000676.2:g.91877621G>A GRCh38
NC_000014.8:g.92343965G>A , CM000676.1:g.92343965G>A GRCh37
NC_000014.7:g.91413718G>A NCBI36
NG_008254.1:g.75082C>T , LRG_364:g.75082C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000557088.6:c.*1017C>T ENSP00000451002.1:n.*1017C>T
ENST00000557570.2:c.883C>T ENSP00000450787.2:p.Arg295Trp
ENST00000706675.1:n.866C>T
ENST00000706676.1:c.1225C>T ENSP00000516492.1:p.Arg409Trp
ENST00000706677.1:c.1051C>T ENSP00000516493.1:p.Arg351Trp
ENST00000706678.1:n.971C>T
ENST00000706679.1:c.883C>T ENSP00000516494.1:p.Arg295Trp
ENST00000706680.1:c.*894C>T ENSP00000516495.1:n.*894C>T
ENST00000706681.1:c.*790C>T ENSP00000516496.1:n.*790C>T
ENST00000342058.9:c.1051C>T MANE Select ENSP00000345008.4:p.Arg351Trp
ENST00000267620.14:c.1174C>T ENSP00000267620.10:p.Arg392Trp
ENST00000342058.8:c.1051C>T ENSP00000345008.4:p.Arg351Trp
ENST00000554121.2:n.177C>T
ENST00000556154.5:c.1066C>T ENSP00000451982.1:p.Arg356Trp
NM_006329.3:c.1051C>T , LRG_364t1:c.1051C>T NP_006320.2:p.Arg351Trp
XM_005267267.3:c.1102C>T XP_005267324.1:p.Arg368Trp
XM_011536356.1:c.1102C>T XP_011534658.1:p.Arg368Trp
XM_011536357.1:c.1051C>T XP_011534659.1:p.Arg351Trp
XM_011536358.1:c.883C>T XP_011534660.1:p.Arg295Trp
XM_011536357.2:c.1051C>T XP_011534659.1:p.Arg351Trp
XM_011536358.2:c.883C>T XP_011534660.1:p.Arg295Trp
XM_017020929.2:c.883C>T XP_016876418.1:p.Arg295Trp
NM_001384158.1:c.1174C>T NP_001371087.1:p.Arg392Trp
NM_001384159.1:c.1102C>T NP_001371088.1:p.Arg368Trp
NM_001384160.1:c.1051C>T NP_001371089.1:p.Arg351Trp
NM_001384161.1:c.883C>T NP_001371090.1:p.Arg295Trp
NM_001384162.1:c.883C>T NP_001371091.1:p.Arg295Trp
NM_006329.4:c.1051C>T MANE Select NP_006320.2:p.Arg351Trp