Canonical Allele Identifier: CA390640732

Gene: FBLN5

Linked Data

• ClinVar Variation Id: 1317179
• ClinVar RCV Id: RCV001759051
• dbSNP Id: rs1802492
• MyVariant Identifiers: chr14:g.92343926C>T (hg19) ; chr14:g.91877582C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91877582C>T , CM000676.2:g.91877582C>T	GRCh38
NC_000014.8:g.92343926C>T , CM000676.1:g.92343926C>T	GRCh37
NC_000014.7:g.91413679C>T	NCBI36
NG_008254.1:g.75121G>A , LRG_364:g.75121G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557088.6:c.*1056G>A	ENSP00000451002.1:n.*1056G>A
ENST00000557570.2:c.922G>A	ENSP00000450787.2:p.Asp308Asn
ENST00000706675.1:n.905G>A
ENST00000706676.1:c.1264G>A	ENSP00000516492.1:p.Asp422Asn
ENST00000706677.1:c.1090G>A	ENSP00000516493.1:p.Asp364Asn
ENST00000706678.1:n.1010G>A
ENST00000706679.1:c.922G>A	ENSP00000516494.1:p.Asp308Asn
ENST00000706680.1:c.*933G>A	ENSP00000516495.1:n.*933G>A
ENST00000706681.1:c.*829G>A	ENSP00000516496.1:n.*829G>A
ENST00000342058.9:c.1090G>A MANE Select	ENSP00000345008.4:p.Asp364Asn
ENST00000267620.14:c.1213G>A	ENSP00000267620.10:p.Asp405Asn
ENST00000342058.8:c.1090G>A	ENSP00000345008.4:p.Asp364Asn
ENST00000554121.2:n.216G>A
ENST00000556154.5:c.1105G>A	ENSP00000451982.1:p.Asp369Asn
NM_006329.3:c.1090G>A , LRG_364t1:c.1090G>A	NP_006320.2:p.Asp364Asn
XM_005267267.3:c.1141G>A	XP_005267324.1:p.Asp381Asn
XM_011536356.1:c.1141G>A	XP_011534658.1:p.Asp381Asn
XM_011536357.1:c.1090G>A	XP_011534659.1:p.Asp364Asn
XM_011536358.1:c.922G>A	XP_011534660.1:p.Asp308Asn
XM_011536357.2:c.1090G>A	XP_011534659.1:p.Asp364Asn
XM_011536358.2:c.922G>A	XP_011534660.1:p.Asp308Asn
XM_017020929.2:c.922G>A	XP_016876418.1:p.Asp308Asn
NM_001384158.1:c.1213G>A	NP_001371087.1:p.Asp405Asn
NM_001384159.1:c.1141G>A	NP_001371088.1:p.Asp381Asn
NM_001384160.1:c.1090G>A	NP_001371089.1:p.Asp364Asn
NM_001384161.1:c.922G>A	NP_001371090.1:p.Asp308Asn
NM_001384162.1:c.922G>A	NP_001371091.1:p.Asp308Asn
NM_006329.4:c.1090G>A MANE Select	NP_006320.2:p.Asp364Asn