Canonical Allele Identifier: CA390642662

Gene: FBLN5

Linked Data

• gnomAD v4: 14-91887255-C-A
• MyVariant Identifiers: chr14:g.92353599C>A (hg19) ; chr14:g.91887255C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91887255C>A , CM000676.2:g.91887255C>A	GRCh38
NC_000014.8:g.92353599C>A , CM000676.1:g.92353599C>A	GRCh37
NC_000014.7:g.91423352C>A	NCBI36
NG_008254.1:g.65448G>T , LRG_364:g.65448G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000557088.6:c.*643G>T	ENSP00000451002.1:n.*643G>T
ENST00000557570.2:c.509G>T	ENSP00000450787.2:p.Gly170Val
ENST00000706676.1:c.851G>T	ENSP00000516492.1:p.Gly284Val
ENST00000706677.1:c.677G>T	ENSP00000516493.1:p.Gly226Val
ENST00000706678.1:n.597G>T
ENST00000706679.1:c.509G>T	ENSP00000516494.1:p.Gly170Val
ENST00000706680.1:c.*520G>T	ENSP00000516495.1:n.*520G>T
ENST00000706681.1:c.*416G>T	ENSP00000516496.1:n.*416G>T
ENST00000342058.9:c.677G>T MANE Select	ENSP00000345008.4:p.Gly226Val
ENST00000267620.14:c.800G>T	ENSP00000267620.10:p.Gly267Val
ENST00000342058.8:c.677G>T	ENSP00000345008.4:p.Gly226Val
ENST00000556154.5:c.692G>T	ENSP00000451982.1:p.Gly231Val
NM_006329.3:c.677G>T , LRG_364t1:c.677G>T	NP_006320.2:p.Gly226Val
XM_005267267.3:c.728G>T	XP_005267324.1:p.Gly243Val
XM_011536356.1:c.728G>T	XP_011534658.1:p.Gly243Val
XM_011536357.1:c.677G>T	XP_011534659.1:p.Gly226Val
XM_011536358.1:c.509G>T	XP_011534660.1:p.Gly170Val
XM_011536357.2:c.677G>T	XP_011534659.1:p.Gly226Val
XM_011536358.2:c.509G>T	XP_011534660.1:p.Gly170Val
XM_017020929.2:c.509G>T	XP_016876418.1:p.Gly170Val
NM_001384158.1:c.800G>T	NP_001371087.1:p.Gly267Val
NM_001384159.1:c.728G>T	NP_001371088.1:p.Gly243Val
NM_001384160.1:c.677G>T	NP_001371089.1:p.Gly226Val
NM_001384161.1:c.509G>T	NP_001371090.1:p.Gly170Val
NM_001384162.1:c.509G>T	NP_001371091.1:p.Gly170Val
NM_006329.4:c.677G>T MANE Select	NP_006320.2:p.Gly226Val