Canonical Allele Identifier: CA2155139552

Gene: FBLN5

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91877635A= , CM000676.2:g.91877635A=	GRCh38
NC_000014.8:g.92343979A= , CM000676.1:g.92343979A=	GRCh37
NC_000014.7:g.91413732A=	NCBI36
NG_008254.1:g.75068T= , LRG_364:g.75068T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557088.6:c.*1003T=	ENSP00000451002.1:n.*1003T=
ENST00000557570.2:c.869T=	ENSP00000450787.2:p.Phe290=
ENST00000706675.1:n.852T=
ENST00000706676.1:c.1211T=	ENSP00000516492.1:p.Phe404=
ENST00000706677.1:c.1037T=	ENSP00000516493.1:p.Phe346=
ENST00000706678.1:n.957T=
ENST00000706679.1:c.869T=	ENSP00000516494.1:p.Phe290=
ENST00000706680.1:c.*880T=	ENSP00000516495.1:n.*880T=
ENST00000706681.1:c.*776T=	ENSP00000516496.1:n.*776T=
ENST00000342058.9:c.1037T= MANE Select	ENSP00000345008.4:p.Phe346=
ENST00000267620.14:c.1160T=	ENSP00000267620.10:p.Phe387=
ENST00000342058.8:c.1037T=	ENSP00000345008.4:p.Phe346=
ENST00000554121.2:n.163T=
ENST00000556154.5:c.1052T=	ENSP00000451982.1:p.Phe351=
NM_006329.3:c.1037T= , LRG_364t1:c.1037T=	NP_006320.2:p.Phe346=
XM_005267267.3:c.1088T=	XP_005267324.1:p.Phe363=
XM_011536356.1:c.1088T=	XP_011534658.1:p.Phe363=
XM_011536357.1:c.1037T=	XP_011534659.1:p.Phe346=
XM_011536358.1:c.869T=	XP_011534660.1:p.Phe290=
XM_011536357.2:c.1037T=	XP_011534659.1:p.Phe346=
XM_011536358.2:c.869T=	XP_011534660.1:p.Phe290=
XM_017020929.2:c.869T=	XP_016876418.1:p.Phe290=
NM_001384158.1:c.1160T=	NP_001371087.1:p.Phe387=
NM_001384159.1:c.1088T=	NP_001371088.1:p.Phe363=
NM_001384160.1:c.1037T=	NP_001371089.1:p.Phe346=
NM_001384161.1:c.869T=	NP_001371090.1:p.Phe290=
NM_001384162.1:c.869T=	NP_001371091.1:p.Phe290=
NM_006329.4:c.1037T= MANE Select	NP_006320.2:p.Phe346=