Canonical Allele Identifier: CA390642674
Gene: FBLN5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91887259A>T , CM000676.2:g.91887259A>T GRCh38
NC_000014.8:g.92353603A>T , CM000676.1:g.92353603A>T GRCh37
NC_000014.7:g.91423356A>T NCBI36
NG_008254.1:g.65444T>A , LRG_364:g.65444T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000557088.6:c.*639T>A ENSP00000451002.1:n.*639T>A
ENST00000557570.2:c.505T>A ENSP00000450787.2:p.Tyr169Asn
ENST00000706676.1:c.847T>A ENSP00000516492.1:p.Tyr283Asn
ENST00000706677.1:c.673T>A ENSP00000516493.1:p.Tyr225Asn
ENST00000706678.1:n.593T>A
ENST00000706679.1:c.505T>A ENSP00000516494.1:p.Tyr169Asn
ENST00000706680.1:c.*516T>A ENSP00000516495.1:n.*516T>A
ENST00000706681.1:c.*412T>A ENSP00000516496.1:n.*412T>A
ENST00000342058.9:c.673T>A MANE Select ENSP00000345008.4:p.Tyr225Asn
ENST00000267620.14:c.796T>A ENSP00000267620.10:p.Tyr266Asn
ENST00000342058.8:c.673T>A ENSP00000345008.4:p.Tyr225Asn
ENST00000556154.5:c.688T>A ENSP00000451982.1:p.Tyr230Asn
NM_006329.3:c.673T>A , LRG_364t1:c.673T>A NP_006320.2:p.Tyr225Asn
XM_005267267.3:c.724T>A XP_005267324.1:p.Tyr242Asn
XM_011536356.1:c.724T>A XP_011534658.1:p.Tyr242Asn
XM_011536357.1:c.673T>A XP_011534659.1:p.Tyr225Asn
XM_011536358.1:c.505T>A XP_011534660.1:p.Tyr169Asn
XM_011536357.2:c.673T>A XP_011534659.1:p.Tyr225Asn
XM_011536358.2:c.505T>A XP_011534660.1:p.Tyr169Asn
XM_017020929.2:c.505T>A XP_016876418.1:p.Tyr169Asn
NM_001384158.1:c.796T>A NP_001371087.1:p.Tyr266Asn
NM_001384159.1:c.724T>A NP_001371088.1:p.Tyr242Asn
NM_001384160.1:c.673T>A NP_001371089.1:p.Tyr225Asn
NM_001384161.1:c.505T>A NP_001371090.1:p.Tyr169Asn
NM_001384162.1:c.505T>A NP_001371091.1:p.Tyr169Asn
NM_006329.4:c.673T>A MANE Select NP_006320.2:p.Tyr225Asn