Canonical Allele Identifier: CA390640513

Gene: FBLN5

Linked Data

• gnomAD v4: 14-91877529-G-C
• MyVariant Identifiers: chr14:g.92343873G>C (hg19) ; chr14:g.91877529G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91877529G>C , CM000676.2:g.91877529G>C	GRCh38
NC_000014.8:g.92343873G>C , CM000676.1:g.92343873G>C	GRCh37
NC_000014.7:g.91413626G>C	NCBI36
NG_008254.1:g.75174C>G , LRG_364:g.75174C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557088.6:c.*1109C>G	ENSP00000451002.1:n.*1109C>G
ENST00000557570.2:c.975C>G	ENSP00000450787.2:p.Phe325Leu
ENST00000706675.1:n.958C>G
ENST00000706676.1:c.1317C>G	ENSP00000516492.1:p.Phe439Leu
ENST00000706677.1:c.1143C>G	ENSP00000516493.1:p.Phe381Leu
ENST00000706678.1:n.1063C>G
ENST00000706679.1:c.975C>G	ENSP00000516494.1:p.Phe325Leu
ENST00000706680.1:c.*986C>G	ENSP00000516495.1:n.*986C>G
ENST00000706681.1:c.*882C>G	ENSP00000516496.1:n.*882C>G
ENST00000342058.9:c.1143C>G MANE Select	ENSP00000345008.4:p.Phe381Leu
ENST00000267620.14:c.1266C>G	ENSP00000267620.10:p.Phe422Leu
ENST00000342058.8:c.1143C>G	ENSP00000345008.4:p.Phe381Leu
ENST00000554121.2:n.269C>G
ENST00000556154.5:c.1158C>G	ENSP00000451982.1:p.Phe386Leu
NM_006329.3:c.1143C>G , LRG_364t1:c.1143C>G	NP_006320.2:p.Phe381Leu
XM_005267267.3:c.1194C>G	XP_005267324.1:p.Phe398Leu
XM_011536356.1:c.1194C>G	XP_011534658.1:p.Phe398Leu
XM_011536357.1:c.1143C>G	XP_011534659.1:p.Phe381Leu
XM_011536358.1:c.975C>G	XP_011534660.1:p.Phe325Leu
XM_011536357.2:c.1143C>G	XP_011534659.1:p.Phe381Leu
XM_011536358.2:c.975C>G	XP_011534660.1:p.Phe325Leu
XM_017020929.2:c.975C>G	XP_016876418.1:p.Phe325Leu
NM_001384158.1:c.1266C>G	NP_001371087.1:p.Phe422Leu
NM_001384159.1:c.1194C>G	NP_001371088.1:p.Phe398Leu
NM_001384160.1:c.1143C>G	NP_001371089.1:p.Phe381Leu
NM_001384161.1:c.975C>G	NP_001371090.1:p.Phe325Leu
NM_001384162.1:c.975C>G	NP_001371091.1:p.Phe325Leu
NM_006329.4:c.1143C>G MANE Select	NP_006320.2:p.Phe381Leu