Canonical Allele Identifier: CA2626159275

Gene: FBLN5

Linked Data

• gnomAD v4: 14-91887162-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91887162G>C , CM000676.2:g.91887162G>C	GRCh38
NC_000014.8:g.92353506G>C , CM000676.1:g.92353506G>C	GRCh37
NC_000014.7:g.91423259G>C	NCBI36
NG_008254.1:g.65541C>G , LRG_364:g.65541C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000557088.6:c.*705+31C>G	ENSP00000451002.1:n.*705+31C>G
ENST00000557570.2:c.571+31C>G	ENSP00000450787.2:n.571+31C>G
ENST00000706676.1:c.913+31C>G	ENSP00000516492.1:n.913+31C>G
ENST00000706677.1:c.739+31C>G	ENSP00000516493.1:n.739+31C>G
ENST00000706678.1:n.659+31C>G
ENST00000706679.1:c.571+31C>G	ENSP00000516494.1:n.571+31C>G
ENST00000706680.1:c.*582+31C>G	ENSP00000516495.1:n.*582+31C>G
ENST00000706681.1:c.*478+31C>G	ENSP00000516496.1:n.*478+31C>G
ENST00000342058.9:c.739+31C>G MANE Select	ENSP00000345008.4:n.739+31C>G
ENST00000267620.14:c.862+31C>G	ENSP00000267620.10:n.862+31C>G
ENST00000342058.8:c.739+31C>G	ENSP00000345008.4:n.739+31C>G
ENST00000556154.5:c.754+31C>G	ENSP00000451982.1:n.754+31C>G
NM_006329.3:c.739+31C>G , LRG_364t1:c.739+31C>G	NP_006320.2:n.739+31C>G
XM_005267267.3:c.790+31C>G	XP_005267324.1:n.790+31C>G
XM_011536356.1:c.790+31C>G	XP_011534658.1:n.790+31C>G
XM_011536357.1:c.739+31C>G	XP_011534659.1:n.739+31C>G
XM_011536358.1:c.571+31C>G	XP_011534660.1:n.571+31C>G
XM_011536357.2:c.739+31C>G	XP_011534659.1:n.739+31C>G
XM_011536358.2:c.571+31C>G	XP_011534660.1:n.571+31C>G
XM_017020929.2:c.571+31C>G	XP_016876418.1:n.571+31C>G
NM_001384158.1:c.862+31C>G	NP_001371087.1:n.862+31C>G
NM_001384159.1:c.790+31C>G	NP_001371088.1:n.790+31C>G
NM_001384160.1:c.739+31C>G	NP_001371089.1:n.739+31C>G
NM_001384161.1:c.571+31C>G	NP_001371090.1:n.571+31C>G
NM_001384162.1:c.571+31C>G	NP_001371091.1:n.571+31C>G
NM_006329.4:c.739+31C>G MANE Select	NP_006320.2:n.739+31C>G