Canonical Allele Identifier: CA2802597404

Gene: FBLN5

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91887457del , CM000676.2:g.91887457del	GRCh38
NC_000014.8:g.92353801del , CM000676.1:g.92353801del	GRCh37
NC_000014.7:g.91423554del	NCBI36
NG_008254.1:g.65248del , LRG_364:g.65248del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557088.6:c.*586-143del	ENSP00000451002.1:n.*586-143del
ENST00000557570.2:c.452-143del	ENSP00000450787.2:n.452-143del
ENST00000706676.1:c.794-143del	ENSP00000516492.1:n.794-143del
ENST00000706677.1:c.620-143del	ENSP00000516493.1:n.620-143del
ENST00000706678.1:n.540-143del
ENST00000706679.1:c.452-143del	ENSP00000516494.1:n.452-143del
ENST00000706680.1:c.*463-143del	ENSP00000516495.1:n.*463-143del
ENST00000706681.1:c.*359-143del	ENSP00000516496.1:n.*359-143del
ENST00000342058.9:c.620-143del MANE Select	ENSP00000345008.4:n.620-143del
ENST00000267620.14:c.743-143del	ENSP00000267620.10:n.743-143del
ENST00000342058.8:c.620-143del	ENSP00000345008.4:n.620-143del
ENST00000556154.5:c.635-143del	ENSP00000451982.1:n.635-143del
NM_006329.3:c.620-143del , LRG_364t1:c.620-143del	NP_006320.2:n.620-143del
XM_005267267.3:c.671-143del	XP_005267324.1:n.671-143del
XM_011536356.1:c.671-143del	XP_011534658.1:n.671-143del
XM_011536357.1:c.620-143del	XP_011534659.1:n.620-143del
XM_011536358.1:c.452-143del	XP_011534660.1:n.452-143del
XM_011536357.2:c.620-143del	XP_011534659.1:n.620-143del
XM_011536358.2:c.452-143del	XP_011534660.1:n.452-143del
XM_017020929.2:c.452-143del	XP_016876418.1:n.452-143del
NM_001384158.1:c.743-143del	NP_001371087.1:n.743-143del
NM_001384159.1:c.671-143del	NP_001371088.1:n.671-143del
NM_001384160.1:c.620-143del	NP_001371089.1:n.620-143del
NM_001384161.1:c.452-143del	NP_001371090.1:n.452-143del
NM_001384162.1:c.452-143del	NP_001371091.1:n.452-143del
NM_006329.4:c.620-143del MANE Select	NP_006320.2:n.620-143del