Canonical Allele Identifier: CA2155133357
Gene: FBLN5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91870346G= , CM000676.2:g.91870346G= GRCh38
NC_000014.8:g.92336690G= , CM000676.1:g.92336690G= GRCh37
NC_000014.7:g.91406443G= NCBI36
NG_008254.1:g.82357C= , LRG_364:g.82357C=

Transcript Alleles

HGVS Amino-acid change
ENST00000557088.6:c.*1191C= ENSP00000451002.1:n.*1191C=
ENST00000557570.2:c.1057C= ENSP00000450787.2:p.Pro353=
ENST00000706675.1:n.1040C=
ENST00000706676.1:c.1399C= ENSP00000516492.1:p.Pro467=
ENST00000706677.1:c.*9C= ENSP00000516493.1:n.*9C=
ENST00000706678.1:n.1145C=
ENST00000706679.1:c.1057C= ENSP00000516494.1:p.Pro353=
ENST00000706680.1:c.*1068C= ENSP00000516495.1:n.*1068C=
ENST00000706681.1:c.*964C= ENSP00000516496.1:n.*964C=
ENST00000342058.9:c.1225C= MANE Select ENSP00000345008.4:p.Pro409=
ENST00000267620.14:c.1348C= ENSP00000267620.10:p.Pro450=
ENST00000342058.8:c.1225C= ENSP00000345008.4:p.Pro409=
ENST00000554121.2:n.351C=
ENST00000556154.5:c.1240C= ENSP00000451982.1:p.Pro414=
ENST00000556961.1:n.1360C=
NM_006329.3:c.1225C= , LRG_364t1:c.1225C= NP_006320.2:p.Pro409=
XM_005267267.3:c.1276C= XP_005267324.1:p.Pro426=
XM_011536356.1:c.*9C= XP_011534658.1:n.*9C=
XM_011536357.1:c.*9C= XP_011534659.1:n.*9C=
XM_011536358.1:c.*9C= XP_011534660.1:n.*9C=
XM_011536357.2:c.*9C= XP_011534659.1:n.*9C=
XM_011536358.2:c.*9C= XP_011534660.1:n.*9C=
XM_017020929.2:c.1057C= XP_016876418.1:p.Pro353=
NM_001384158.1:c.1348C= NP_001371087.1:p.Pro450=
NM_001384159.1:c.1276C= NP_001371088.1:p.Pro426=
NM_001384160.1:c.*9C= NP_001371089.1:n.*9C=
NM_001384161.1:c.*9C= NP_001371090.1:n.*9C=
NM_001384162.1:c.1057C= NP_001371091.1:p.Pro353=
NM_006329.4:c.1225C= MANE Select NP_006320.2:p.Pro409=