Canonical Allele Identifier: CA487566709

Gene: FBLN5

Linked Data

• MyVariant Identifiers: chr14:g.92343906G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91877562G>A , CM000676.2:g.91877562G>A	GRCh38
NC_000014.8:g.92343906G>A , CM000676.1:g.92343906G>A	GRCh37
NC_000014.7:g.91413659G>A	NCBI36
NG_008254.1:g.75141C>T , LRG_364:g.75141C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557088.6:c.*1076C>T	ENSP00000451002.1:n.*1076C>T
ENST00000557570.2:c.942C>T	ENSP00000450787.2:p.Ala314=
ENST00000706675.1:n.925C>T
ENST00000706676.1:c.1284C>T	ENSP00000516492.1:p.Ala428=
ENST00000706677.1:c.1110C>T	ENSP00000516493.1:p.Ala370=
ENST00000706678.1:n.1030C>T
ENST00000706679.1:c.942C>T	ENSP00000516494.1:p.Ala314=
ENST00000706680.1:c.*953C>T	ENSP00000516495.1:n.*953C>T
ENST00000706681.1:c.*849C>T	ENSP00000516496.1:n.*849C>T
ENST00000342058.9:c.1110C>T MANE Select	ENSP00000345008.4:p.Ala370=
ENST00000267620.14:c.1233C>T	ENSP00000267620.10:p.Ala411=
ENST00000342058.8:c.1110C>T	ENSP00000345008.4:p.Ala370=
ENST00000554121.2:n.236C>T
ENST00000556154.5:c.1125C>T	ENSP00000451982.1:p.Ala375=
NM_006329.3:c.1110C>T , LRG_364t1:c.1110C>T	NP_006320.2:p.Ala370=
XM_005267267.3:c.1161C>T	XP_005267324.1:p.Ala387=
XM_011536356.1:c.1161C>T	XP_011534658.1:p.Ala387=
XM_011536357.1:c.1110C>T	XP_011534659.1:p.Ala370=
XM_011536358.1:c.942C>T	XP_011534660.1:p.Ala314=
XM_011536357.2:c.1110C>T	XP_011534659.1:p.Ala370=
XM_011536358.2:c.942C>T	XP_011534660.1:p.Ala314=
XM_017020929.2:c.942C>T	XP_016876418.1:p.Ala314=
NM_001384158.1:c.1233C>T	NP_001371087.1:p.Ala411=
NM_001384159.1:c.1161C>T	NP_001371088.1:p.Ala387=
NM_001384160.1:c.1110C>T	NP_001371089.1:p.Ala370=
NM_001384161.1:c.942C>T	NP_001371090.1:p.Ala314=
NM_001384162.1:c.942C>T	NP_001371091.1:p.Ala314=
NM_006329.4:c.1110C>T MANE Select	NP_006320.2:p.Ala370=