Canonical Allele Identifier: CA390642710

Gene: FBLN5

Linked Data

• MyVariant Identifiers: chr14:g.92353620T>C (hg19) ; chr14:g.91887276T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91887276T>C , CM000676.2:g.91887276T>C	GRCh38
NC_000014.8:g.92353620T>C , CM000676.1:g.92353620T>C	GRCh37
NC_000014.7:g.91423373T>C	NCBI36
NG_008254.1:g.65427A>G , LRG_364:g.65427A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557088.6:c.*622A>G	ENSP00000451002.1:n.*622A>G
ENST00000557570.2:c.488A>G	ENSP00000450787.2:p.Gln163Arg
ENST00000706676.1:c.830A>G	ENSP00000516492.1:p.Gln277Arg
ENST00000706677.1:c.656A>G	ENSP00000516493.1:p.Gln219Arg
ENST00000706678.1:n.576A>G
ENST00000706679.1:c.488A>G	ENSP00000516494.1:p.Gln163Arg
ENST00000706680.1:c.*499A>G	ENSP00000516495.1:n.*499A>G
ENST00000706681.1:c.*395A>G	ENSP00000516496.1:n.*395A>G
ENST00000342058.9:c.656A>G MANE Select	ENSP00000345008.4:p.Gln219Arg
ENST00000267620.14:c.779A>G	ENSP00000267620.10:p.Gln260Arg
ENST00000342058.8:c.656A>G	ENSP00000345008.4:p.Gln219Arg
ENST00000556154.5:c.671A>G	ENSP00000451982.1:p.Gln224Arg
NM_006329.3:c.656A>G , LRG_364t1:c.656A>G	NP_006320.2:p.Gln219Arg
XM_005267267.3:c.707A>G	XP_005267324.1:p.Gln236Arg
XM_011536356.1:c.707A>G	XP_011534658.1:p.Gln236Arg
XM_011536357.1:c.656A>G	XP_011534659.1:p.Gln219Arg
XM_011536358.1:c.488A>G	XP_011534660.1:p.Gln163Arg
XM_011536357.2:c.656A>G	XP_011534659.1:p.Gln219Arg
XM_011536358.2:c.488A>G	XP_011534660.1:p.Gln163Arg
XM_017020929.2:c.488A>G	XP_016876418.1:p.Gln163Arg
NM_001384158.1:c.779A>G	NP_001371087.1:p.Gln260Arg
NM_001384159.1:c.707A>G	NP_001371088.1:p.Gln236Arg
NM_001384160.1:c.656A>G	NP_001371089.1:p.Gln219Arg
NM_001384161.1:c.488A>G	NP_001371090.1:p.Gln163Arg
NM_001384162.1:c.488A>G	NP_001371091.1:p.Gln163Arg
NM_006329.4:c.656A>G MANE Select	NP_006320.2:p.Gln219Arg