Canonical Allele Identifier: CA390640443

Gene: FBLN5

Linked Data

• MyVariant Identifiers: chr14:g.92343842A>T (hg19) ; chr14:g.91877498A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91877498A>T , CM000676.2:g.91877498A>T	GRCh38
NC_000014.8:g.92343842A>T , CM000676.1:g.92343842A>T	GRCh37
NC_000014.7:g.91413595A>T	NCBI36
NG_008254.1:g.75205T>A , LRG_364:g.75205T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000557088.6:c.*1140T>A	ENSP00000451002.1:n.*1140T>A
ENST00000557570.2:c.1006T>A	ENSP00000450787.2:p.Phe336Ile
ENST00000706675.1:n.989T>A
ENST00000706676.1:c.1348T>A	ENSP00000516492.1:p.Phe450Ile
ENST00000706677.1:c.1174T>A	ENSP00000516493.1:p.Phe392Ile
ENST00000706678.1:n.1094T>A
ENST00000706679.1:c.1006T>A	ENSP00000516494.1:p.Phe336Ile
ENST00000706680.1:c.*1017T>A	ENSP00000516495.1:n.*1017T>A
ENST00000706681.1:c.*913T>A	ENSP00000516496.1:n.*913T>A
ENST00000342058.9:c.1174T>A MANE Select	ENSP00000345008.4:p.Phe392Ile
ENST00000267620.14:c.1297T>A	ENSP00000267620.10:p.Phe433Ile
ENST00000342058.8:c.1174T>A	ENSP00000345008.4:p.Phe392Ile
ENST00000554121.2:n.300T>A
ENST00000556154.5:c.1189T>A	ENSP00000451982.1:p.Phe397Ile
NM_006329.3:c.1174T>A , LRG_364t1:c.1174T>A	NP_006320.2:p.Phe392Ile
XM_005267267.3:c.1225T>A	XP_005267324.1:p.Phe409Ile
XM_011536356.1:c.1225T>A	XP_011534658.1:p.Phe409Ile
XM_011536357.1:c.1174T>A	XP_011534659.1:p.Phe392Ile
XM_011536358.1:c.1006T>A	XP_011534660.1:p.Phe336Ile
XM_011536357.2:c.1174T>A	XP_011534659.1:p.Phe392Ile
XM_011536358.2:c.1006T>A	XP_011534660.1:p.Phe336Ile
XM_017020929.2:c.1006T>A	XP_016876418.1:p.Phe336Ile
NM_001384158.1:c.1297T>A	NP_001371087.1:p.Phe433Ile
NM_001384159.1:c.1225T>A	NP_001371088.1:p.Phe409Ile
NM_001384160.1:c.1174T>A	NP_001371089.1:p.Phe392Ile
NM_001384161.1:c.1006T>A	NP_001371090.1:p.Phe336Ile
NM_001384162.1:c.1006T>A	NP_001371091.1:p.Phe336Ile
NM_006329.4:c.1174T>A MANE Select	NP_006320.2:p.Phe392Ile