Canonical Allele Identifier: CA390641172

Gene: FBLN5

Linked Data

• MyVariant Identifiers: chr14:g.92344024C>G (hg19) ; chr14:g.91877680C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91877680C>G , CM000676.2:g.91877680C>G	GRCh38
NC_000014.8:g.92344024C>G , CM000676.1:g.92344024C>G	GRCh37
NC_000014.7:g.91413777C>G	NCBI36
NG_008254.1:g.75023G>C , LRG_364:g.75023G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557088.6:c.*958G>C	ENSP00000451002.1:n.*958G>C
ENST00000557570.2:c.824G>C	ENSP00000450787.2:p.Arg275Pro
ENST00000706675.1:n.807G>C
ENST00000706676.1:c.1166G>C	ENSP00000516492.1:p.Arg389Pro
ENST00000706677.1:c.992G>C	ENSP00000516493.1:p.Arg331Pro
ENST00000706678.1:n.912G>C
ENST00000706679.1:c.824G>C	ENSP00000516494.1:p.Arg275Pro
ENST00000706680.1:c.*835G>C	ENSP00000516495.1:n.*835G>C
ENST00000706681.1:c.*731G>C	ENSP00000516496.1:n.*731G>C
ENST00000342058.9:c.992G>C MANE Select	ENSP00000345008.4:p.Arg331Pro
ENST00000267620.14:c.1115G>C	ENSP00000267620.10:p.Arg372Pro
ENST00000342058.8:c.992G>C	ENSP00000345008.4:p.Arg331Pro
ENST00000554121.2:n.118G>C
ENST00000556154.5:c.1007G>C	ENSP00000451982.1:p.Arg336Pro
NM_006329.3:c.992G>C , LRG_364t1:c.992G>C	NP_006320.2:p.Arg331Pro
XM_005267267.3:c.1043G>C	XP_005267324.1:p.Arg348Pro
XM_011536356.1:c.1043G>C	XP_011534658.1:p.Arg348Pro
XM_011536357.1:c.992G>C	XP_011534659.1:p.Arg331Pro
XM_011536358.1:c.824G>C	XP_011534660.1:p.Arg275Pro
XM_011536357.2:c.992G>C	XP_011534659.1:p.Arg331Pro
XM_011536358.2:c.824G>C	XP_011534660.1:p.Arg275Pro
XM_017020929.2:c.824G>C	XP_016876418.1:p.Arg275Pro
NM_001384158.1:c.1115G>C	NP_001371087.1:p.Arg372Pro
NM_001384159.1:c.1043G>C	NP_001371088.1:p.Arg348Pro
NM_001384160.1:c.992G>C	NP_001371089.1:p.Arg331Pro
NM_001384161.1:c.824G>C	NP_001371090.1:p.Arg275Pro
NM_001384162.1:c.824G>C	NP_001371091.1:p.Arg275Pro
NM_006329.4:c.992G>C MANE Select	NP_006320.2:p.Arg331Pro