Canonical Allele Identifier: CA390640872

Gene: FBLN5

Linked Data

• ClinVar Variation Id: 2797677
• ClinVar RCV Id: RCV003673342
• gnomAD v4: 14-91877615-T-C
• MyVariant Identifiers: chr14:g.92343959T>C (hg19) ; chr14:g.91877615T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91877615T>C , CM000676.2:g.91877615T>C	GRCh38
NC_000014.8:g.92343959T>C , CM000676.1:g.92343959T>C	GRCh37
NC_000014.7:g.91413712T>C	NCBI36
NG_008254.1:g.75088A>G , LRG_364:g.75088A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557088.6:c.*1023A>G	ENSP00000451002.1:n.*1023A>G
ENST00000557570.2:c.889A>G	ENSP00000450787.2:p.Met297Val
ENST00000706675.1:n.872A>G
ENST00000706676.1:c.1231A>G	ENSP00000516492.1:p.Met411Val
ENST00000706677.1:c.1057A>G	ENSP00000516493.1:p.Met353Val
ENST00000706678.1:n.977A>G
ENST00000706679.1:c.889A>G	ENSP00000516494.1:p.Met297Val
ENST00000706680.1:c.*900A>G	ENSP00000516495.1:n.*900A>G
ENST00000706681.1:c.*796A>G	ENSP00000516496.1:n.*796A>G
ENST00000342058.9:c.1057A>G MANE Select	ENSP00000345008.4:p.Met353Val
ENST00000267620.14:c.1180A>G	ENSP00000267620.10:p.Met394Val
ENST00000342058.8:c.1057A>G	ENSP00000345008.4:p.Met353Val
ENST00000554121.2:n.183A>G
ENST00000556154.5:c.1072A>G	ENSP00000451982.1:p.Met358Val
NM_006329.3:c.1057A>G , LRG_364t1:c.1057A>G	NP_006320.2:p.Met353Val
XM_005267267.3:c.1108A>G	XP_005267324.1:p.Met370Val
XM_011536356.1:c.1108A>G	XP_011534658.1:p.Met370Val
XM_011536357.1:c.1057A>G	XP_011534659.1:p.Met353Val
XM_011536358.1:c.889A>G	XP_011534660.1:p.Met297Val
XM_011536357.2:c.1057A>G	XP_011534659.1:p.Met353Val
XM_011536358.2:c.889A>G	XP_011534660.1:p.Met297Val
XM_017020929.2:c.889A>G	XP_016876418.1:p.Met297Val
NM_001384158.1:c.1180A>G	NP_001371087.1:p.Met394Val
NM_001384159.1:c.1108A>G	NP_001371088.1:p.Met370Val
NM_001384160.1:c.1057A>G	NP_001371089.1:p.Met353Val
NM_001384161.1:c.889A>G	NP_001371090.1:p.Met297Val
NM_001384162.1:c.889A>G	NP_001371091.1:p.Met297Val
NM_006329.4:c.1057A>G MANE Select	NP_006320.2:p.Met353Val