Canonical Allele Identifier: CA487566419

Gene: FBLN5

Linked Data

• MyVariant Identifiers: chr14:g.92336688G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91870344G>C , CM000676.2:g.91870344G>C	GRCh38
NC_000014.8:g.92336688G>C , CM000676.1:g.92336688G>C	GRCh37
NC_000014.7:g.91406441G>C	NCBI36
NG_008254.1:g.82359C>G , LRG_364:g.82359C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000557088.6:c.*1193C>G	ENSP00000451002.1:n.*1193C>G
ENST00000557570.2:c.1059C>G	ENSP00000450787.2:p.Pro353=
ENST00000706675.1:n.1042C>G
ENST00000706676.1:c.1401C>G	ENSP00000516492.1:p.Pro467=
ENST00000706677.1:c.*11C>G	ENSP00000516493.1:n.*11C>G
ENST00000706678.1:n.1147C>G
ENST00000706679.1:c.1059C>G	ENSP00000516494.1:p.Pro353=
ENST00000706680.1:c.*1070C>G	ENSP00000516495.1:n.*1070C>G
ENST00000706681.1:c.*966C>G	ENSP00000516496.1:n.*966C>G
ENST00000342058.9:c.1227C>G MANE Select	ENSP00000345008.4:p.Pro409=
ENST00000267620.14:c.1350C>G	ENSP00000267620.10:p.Pro450=
ENST00000342058.8:c.1227C>G	ENSP00000345008.4:p.Pro409=
ENST00000554121.2:n.353C>G
ENST00000556154.5:c.1242C>G	ENSP00000451982.1:p.Pro414=
ENST00000556961.1:n.1362C>G
NM_006329.3:c.1227C>G , LRG_364t1:c.1227C>G	NP_006320.2:p.Pro409=
XM_005267267.3:c.1278C>G	XP_005267324.1:p.Pro426=
XM_011536356.1:c.*11C>G	XP_011534658.1:n.*11C>G
XM_011536357.1:c.*11C>G	XP_011534659.1:n.*11C>G
XM_011536358.1:c.*11C>G	XP_011534660.1:n.*11C>G
XM_011536357.2:c.*11C>G	XP_011534659.1:n.*11C>G
XM_011536358.2:c.*11C>G	XP_011534660.1:n.*11C>G
XM_017020929.2:c.1059C>G	XP_016876418.1:p.Pro353=
NM_001384158.1:c.1350C>G	NP_001371087.1:p.Pro450=
NM_001384159.1:c.1278C>G	NP_001371088.1:p.Pro426=
NM_001384160.1:c.*11C>G	NP_001371089.1:n.*11C>G
NM_001384161.1:c.*11C>G	NP_001371090.1:n.*11C>G
NM_001384162.1:c.1059C>G	NP_001371091.1:p.Pro353=
NM_006329.4:c.1227C>G MANE Select	NP_006320.2:p.Pro409=