Canonical Allele Identifier: CA390639384
Gene: FBLN5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91870339T>A , CM000676.2:g.91870339T>A GRCh38
NC_000014.8:g.92336683T>A , CM000676.1:g.92336683T>A GRCh37
NC_000014.7:g.91406436T>A NCBI36
NG_008254.1:g.82364A>T , LRG_364:g.82364A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000557088.6:c.*1198A>T ENSP00000451002.1:n.*1198A>T
ENST00000557570.2:c.1064A>T ENSP00000450787.2:p.Lys355Ile
ENST00000706675.1:n.1047A>T
ENST00000706676.1:c.1406A>T ENSP00000516492.1:p.Lys469Ile
ENST00000706677.1:c.*16A>T ENSP00000516493.1:n.*16A>T
ENST00000706678.1:n.1152A>T
ENST00000706679.1:c.1064A>T ENSP00000516494.1:p.Lys355Ile
ENST00000706680.1:c.*1075A>T ENSP00000516495.1:n.*1075A>T
ENST00000706681.1:c.*971A>T ENSP00000516496.1:n.*971A>T
ENST00000342058.9:c.1232A>T MANE Select ENSP00000345008.4:p.Lys411Ile
ENST00000267620.14:c.1355A>T ENSP00000267620.10:p.Lys452Ile
ENST00000342058.8:c.1232A>T ENSP00000345008.4:p.Lys411Ile
ENST00000554121.2:n.358A>T
ENST00000556154.5:c.1247A>T ENSP00000451982.1:p.Lys416Ile
ENST00000556961.1:n.1367A>T
NM_006329.3:c.1232A>T , LRG_364t1:c.1232A>T NP_006320.2:p.Lys411Ile
XM_005267267.3:c.1283A>T XP_005267324.1:p.Lys428Ile
XM_011536356.1:c.*16A>T XP_011534658.1:n.*16A>T
XM_011536357.1:c.*16A>T XP_011534659.1:n.*16A>T
XM_011536358.1:c.*16A>T XP_011534660.1:n.*16A>T
XM_011536357.2:c.*16A>T XP_011534659.1:n.*16A>T
XM_011536358.2:c.*16A>T XP_011534660.1:n.*16A>T
XM_017020929.2:c.1064A>T XP_016876418.1:p.Lys355Ile
NM_001384158.1:c.1355A>T NP_001371087.1:p.Lys452Ile
NM_001384159.1:c.1283A>T NP_001371088.1:p.Lys428Ile
NM_001384160.1:c.*16A>T NP_001371089.1:n.*16A>T
NM_001384161.1:c.*16A>T NP_001371090.1:n.*16A>T
NM_001384162.1:c.1064A>T NP_001371091.1:p.Lys355Ile
NM_006329.4:c.1232A>T MANE Select NP_006320.2:p.Lys411Ile