Canonical Allele Identifier: CA390640530

Gene: FBLN5

Linked Data

• MyVariant Identifiers: chr14:g.92343880T>C (hg19) ; chr14:g.91877536T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91877536T>C , CM000676.2:g.91877536T>C	GRCh38
NC_000014.8:g.92343880T>C , CM000676.1:g.92343880T>C	GRCh37
NC_000014.7:g.91413633T>C	NCBI36
NG_008254.1:g.75167A>G , LRG_364:g.75167A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557088.6:c.*1102A>G	ENSP00000451002.1:n.*1102A>G
ENST00000557570.2:c.968A>G	ENSP00000450787.2:p.Tyr323Cys
ENST00000706675.1:n.951A>G
ENST00000706676.1:c.1310A>G	ENSP00000516492.1:p.Tyr437Cys
ENST00000706677.1:c.1136A>G	ENSP00000516493.1:p.Tyr379Cys
ENST00000706678.1:n.1056A>G
ENST00000706679.1:c.968A>G	ENSP00000516494.1:p.Tyr323Cys
ENST00000706680.1:c.*979A>G	ENSP00000516495.1:n.*979A>G
ENST00000706681.1:c.*875A>G	ENSP00000516496.1:n.*875A>G
ENST00000342058.9:c.1136A>G MANE Select	ENSP00000345008.4:p.Tyr379Cys
ENST00000267620.14:c.1259A>G	ENSP00000267620.10:p.Tyr420Cys
ENST00000342058.8:c.1136A>G	ENSP00000345008.4:p.Tyr379Cys
ENST00000554121.2:n.262A>G
ENST00000556154.5:c.1151A>G	ENSP00000451982.1:p.Tyr384Cys
NM_006329.3:c.1136A>G , LRG_364t1:c.1136A>G	NP_006320.2:p.Tyr379Cys
XM_005267267.3:c.1187A>G	XP_005267324.1:p.Tyr396Cys
XM_011536356.1:c.1187A>G	XP_011534658.1:p.Tyr396Cys
XM_011536357.1:c.1136A>G	XP_011534659.1:p.Tyr379Cys
XM_011536358.1:c.968A>G	XP_011534660.1:p.Tyr323Cys
XM_011536357.2:c.1136A>G	XP_011534659.1:p.Tyr379Cys
XM_011536358.2:c.968A>G	XP_011534660.1:p.Tyr323Cys
XM_017020929.2:c.968A>G	XP_016876418.1:p.Tyr323Cys
NM_001384158.1:c.1259A>G	NP_001371087.1:p.Tyr420Cys
NM_001384159.1:c.1187A>G	NP_001371088.1:p.Tyr396Cys
NM_001384160.1:c.1136A>G	NP_001371089.1:p.Tyr379Cys
NM_001384161.1:c.968A>G	NP_001371090.1:p.Tyr323Cys
NM_001384162.1:c.968A>G	NP_001371091.1:p.Tyr323Cys
NM_006329.4:c.1136A>G MANE Select	NP_006320.2:p.Tyr379Cys