Canonical Allele Identifier: CA487566349

Gene: FBLN5

Linked Data

• MyVariant Identifiers: chr14:g.92336586C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91870242C>G , CM000676.2:g.91870242C>G	GRCh38
NC_000014.8:g.92336586C>G , CM000676.1:g.92336586C>G	GRCh37
NC_000014.7:g.91406339C>G	NCBI36
NG_008254.1:g.82461G>C , LRG_364:g.82461G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557088.6:c.*1295G>C	ENSP00000451002.1:n.*1295G>C
ENST00000557570.2:c.1161G>C	ENSP00000450787.2:p.Val387=
ENST00000706675.1:n.1144G>C
ENST00000706676.1:c.1503G>C	ENSP00000516492.1:p.Val501=
ENST00000706677.1:c.*113G>C	ENSP00000516493.1:n.*113G>C
ENST00000706678.1:n.1249G>C
ENST00000706679.1:c.1161G>C	ENSP00000516494.1:p.Val387=
ENST00000706680.1:c.*1172G>C	ENSP00000516495.1:n.*1172G>C
ENST00000706681.1:c.*1068G>C	ENSP00000516496.1:n.*1068G>C
ENST00000342058.9:c.1329G>C MANE Select	ENSP00000345008.4:p.Val443=
ENST00000267620.14:c.1452G>C	ENSP00000267620.10:p.Val484=
ENST00000342058.8:c.1329G>C	ENSP00000345008.4:p.Val443=
ENST00000554121.2:n.455G>C
ENST00000556154.5:c.1344G>C	ENSP00000451982.1:p.Val448=
ENST00000556961.1:n.1464G>C
NM_006329.3:c.1329G>C , LRG_364t1:c.1329G>C	NP_006320.2:p.Val443=
XM_005267267.3:c.1380G>C	XP_005267324.1:p.Val460=
XM_011536356.1:c.*113G>C	XP_011534658.1:n.*113G>C
XM_011536357.1:c.*113G>C	XP_011534659.1:n.*113G>C
XM_011536358.1:c.*113G>C	XP_011534660.1:n.*113G>C
XM_011536357.2:c.*113G>C	XP_011534659.1:n.*113G>C
XM_011536358.2:c.*113G>C	XP_011534660.1:n.*113G>C
XM_017020929.2:c.1161G>C	XP_016876418.1:p.Val387=
NM_001384158.1:c.1452G>C	NP_001371087.1:p.Val484=
NM_001384159.1:c.1380G>C	NP_001371088.1:p.Val460=
NM_001384160.1:c.*113G>C	NP_001371089.1:n.*113G>C
NM_001384161.1:c.*113G>C	NP_001371090.1:n.*113G>C
NM_001384162.1:c.1161G>C	NP_001371091.1:p.Val387=
NM_006329.4:c.1329G>C MANE Select	NP_006320.2:p.Val443=