Canonical Allele Identifier: CA390639296

Gene: FBLN5

Linked Data

• MyVariant Identifiers: chr14:g.92336660C>T (hg19) ; chr14:g.91870316C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91870316C>T , CM000676.2:g.91870316C>T	GRCh38
NC_000014.8:g.92336660C>T , CM000676.1:g.92336660C>T	GRCh37
NC_000014.7:g.91406413C>T	NCBI36
NG_008254.1:g.82387G>A , LRG_364:g.82387G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557088.6:c.*1221G>A	ENSP00000451002.1:n.*1221G>A
ENST00000557570.2:c.1087G>A	ENSP00000450787.2:p.Asp363Asn
ENST00000706675.1:n.1070G>A
ENST00000706676.1:c.1429G>A	ENSP00000516492.1:p.Asp477Asn
ENST00000706677.1:c.*39G>A	ENSP00000516493.1:n.*39G>A
ENST00000706678.1:n.1175G>A
ENST00000706679.1:c.1087G>A	ENSP00000516494.1:p.Asp363Asn
ENST00000706680.1:c.*1098G>A	ENSP00000516495.1:n.*1098G>A
ENST00000706681.1:c.*994G>A	ENSP00000516496.1:n.*994G>A
ENST00000342058.9:c.1255G>A MANE Select	ENSP00000345008.4:p.Asp419Asn
ENST00000267620.14:c.1378G>A	ENSP00000267620.10:p.Asp460Asn
ENST00000342058.8:c.1255G>A	ENSP00000345008.4:p.Asp419Asn
ENST00000554121.2:n.381G>A
ENST00000556154.5:c.1270G>A	ENSP00000451982.1:p.Asp424Asn
ENST00000556961.1:n.1390G>A
NM_006329.3:c.1255G>A , LRG_364t1:c.1255G>A	NP_006320.2:p.Asp419Asn
XM_005267267.3:c.1306G>A	XP_005267324.1:p.Asp436Asn
XM_011536356.1:c.*39G>A	XP_011534658.1:n.*39G>A
XM_011536357.1:c.*39G>A	XP_011534659.1:n.*39G>A
XM_011536358.1:c.*39G>A	XP_011534660.1:n.*39G>A
XM_011536357.2:c.*39G>A	XP_011534659.1:n.*39G>A
XM_011536358.2:c.*39G>A	XP_011534660.1:n.*39G>A
XM_017020929.2:c.1087G>A	XP_016876418.1:p.Asp363Asn
NM_001384158.1:c.1378G>A	NP_001371087.1:p.Asp460Asn
NM_001384159.1:c.1306G>A	NP_001371088.1:p.Asp436Asn
NM_001384160.1:c.*39G>A	NP_001371089.1:n.*39G>A
NM_001384161.1:c.*39G>A	NP_001371090.1:n.*39G>A
NM_001384162.1:c.1087G>A	NP_001371091.1:p.Asp363Asn
NM_006329.4:c.1255G>A MANE Select	NP_006320.2:p.Asp419Asn