Canonical Allele Identifier: CA2155139423

Gene: FBLN5

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91877559C= , CM000676.2:g.91877559C=	GRCh38
NC_000014.8:g.92343903C= , CM000676.1:g.92343903C=	GRCh37
NC_000014.7:g.91413656C=	NCBI36
NG_008254.1:g.75144G= , LRG_364:g.75144G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557088.6:c.*1079G=	ENSP00000451002.1:n.*1079G=
ENST00000557570.2:c.945G=	ENSP00000450787.2:p.Thr315=
ENST00000706675.1:n.928G=
ENST00000706676.1:c.1287G=	ENSP00000516492.1:p.Thr429=
ENST00000706677.1:c.1113G=	ENSP00000516493.1:p.Thr371=
ENST00000706678.1:n.1033G=
ENST00000706679.1:c.945G=	ENSP00000516494.1:p.Thr315=
ENST00000706680.1:c.*956G=	ENSP00000516495.1:n.*956G=
ENST00000706681.1:c.*852G=	ENSP00000516496.1:n.*852G=
ENST00000342058.9:c.1113G= MANE Select	ENSP00000345008.4:p.Thr371=
ENST00000267620.14:c.1236G=	ENSP00000267620.10:p.Thr412=
ENST00000342058.8:c.1113G=	ENSP00000345008.4:p.Thr371=
ENST00000554121.2:n.239G=
ENST00000556154.5:c.1128G=	ENSP00000451982.1:p.Thr376=
NM_006329.3:c.1113G= , LRG_364t1:c.1113G=	NP_006320.2:p.Thr371=
XM_005267267.3:c.1164G=	XP_005267324.1:p.Thr388=
XM_011536356.1:c.1164G=	XP_011534658.1:p.Thr388=
XM_011536357.1:c.1113G=	XP_011534659.1:p.Thr371=
XM_011536358.1:c.945G=	XP_011534660.1:p.Thr315=
XM_011536357.2:c.1113G=	XP_011534659.1:p.Thr371=
XM_011536358.2:c.945G=	XP_011534660.1:p.Thr315=
XM_017020929.2:c.945G=	XP_016876418.1:p.Thr315=
NM_001384158.1:c.1236G=	NP_001371087.1:p.Thr412=
NM_001384159.1:c.1164G=	NP_001371088.1:p.Thr388=
NM_001384160.1:c.1113G=	NP_001371089.1:p.Thr371=
NM_001384161.1:c.945G=	NP_001371090.1:p.Thr315=
NM_001384162.1:c.945G=	NP_001371091.1:p.Thr315=
NM_006329.4:c.1113G= MANE Select	NP_006320.2:p.Thr371=