Canonical Allele Identifier: CA390641108

Gene: FBLN5

Linked Data

• ClinVar Variation Id: 3012747
• ClinVar RCV Id: RCV003877858
• MyVariant Identifiers: chr14:g.92344012G>A (hg19) ; chr14:g.91877668G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91877668G>A , CM000676.2:g.91877668G>A	GRCh38
NC_000014.8:g.92344012G>A , CM000676.1:g.92344012G>A	GRCh37
NC_000014.7:g.91413765G>A	NCBI36
NG_008254.1:g.75035C>T , LRG_364:g.75035C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557088.6:c.*970C>T	ENSP00000451002.1:n.*970C>T
ENST00000557570.2:c.836C>T	ENSP00000450787.2:p.Pro279Leu
ENST00000706675.1:n.819C>T
ENST00000706676.1:c.1178C>T	ENSP00000516492.1:p.Pro393Leu
ENST00000706677.1:c.1004C>T	ENSP00000516493.1:p.Pro335Leu
ENST00000706678.1:n.924C>T
ENST00000706679.1:c.836C>T	ENSP00000516494.1:p.Pro279Leu
ENST00000706680.1:c.*847C>T	ENSP00000516495.1:n.*847C>T
ENST00000706681.1:c.*743C>T	ENSP00000516496.1:n.*743C>T
ENST00000342058.9:c.1004C>T MANE Select	ENSP00000345008.4:p.Pro335Leu
ENST00000267620.14:c.1127C>T	ENSP00000267620.10:p.Pro376Leu
ENST00000342058.8:c.1004C>T	ENSP00000345008.4:p.Pro335Leu
ENST00000554121.2:n.130C>T
ENST00000556154.5:c.1019C>T	ENSP00000451982.1:p.Pro340Leu
NM_006329.3:c.1004C>T , LRG_364t1:c.1004C>T	NP_006320.2:p.Pro335Leu
XM_005267267.3:c.1055C>T	XP_005267324.1:p.Pro352Leu
XM_011536356.1:c.1055C>T	XP_011534658.1:p.Pro352Leu
XM_011536357.1:c.1004C>T	XP_011534659.1:p.Pro335Leu
XM_011536358.1:c.836C>T	XP_011534660.1:p.Pro279Leu
XM_011536357.2:c.1004C>T	XP_011534659.1:p.Pro335Leu
XM_011536358.2:c.836C>T	XP_011534660.1:p.Pro279Leu
XM_017020929.2:c.836C>T	XP_016876418.1:p.Pro279Leu
NM_001384158.1:c.1127C>T	NP_001371087.1:p.Pro376Leu
NM_001384159.1:c.1055C>T	NP_001371088.1:p.Pro352Leu
NM_001384160.1:c.1004C>T	NP_001371089.1:p.Pro335Leu
NM_001384161.1:c.836C>T	NP_001371090.1:p.Pro279Leu
NM_001384162.1:c.836C>T	NP_001371091.1:p.Pro279Leu
NM_006329.4:c.1004C>T MANE Select	NP_006320.2:p.Pro335Leu