Canonical Allele Identifier: CA2155159010

Gene: FBLN5

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91891236C= , CM000676.2:g.91891236C=	GRCh38
NC_000014.8:g.92357580C= , CM000676.1:g.92357580C=	GRCh37
NC_000014.7:g.91427333C=	NCBI36
NG_008254.1:g.61467G= , LRG_364:g.61467G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557088.6:c.*570G=	ENSP00000451002.1:n.*570G=
ENST00000557570.2:c.436G=	ENSP00000450787.2:p.Gly146=
ENST00000706676.1:c.778G=	ENSP00000516492.1:p.Gly260=
ENST00000706677.1:c.604G=	ENSP00000516493.1:p.Gly202=
ENST00000706678.1:n.524G=
ENST00000706679.1:c.436G=	ENSP00000516494.1:p.Gly146=
ENST00000706680.1:c.*447G=	ENSP00000516495.1:n.*447G=
ENST00000706681.1:c.*343G=	ENSP00000516496.1:n.*343G=
ENST00000342058.9:c.604G= MANE Select	ENSP00000345008.4:p.Gly202=
ENST00000267620.14:c.727G=	ENSP00000267620.10:p.Gly243=
ENST00000342058.8:c.604G=	ENSP00000345008.4:p.Gly202=
ENST00000556154.5:c.619G=	ENSP00000451982.1:p.Gly207=
NM_006329.3:c.604G= , LRG_364t1:c.604G=	NP_006320.2:p.Gly202=
XM_005267267.3:c.655G=	XP_005267324.1:p.Gly219=
XM_011536356.1:c.655G=	XP_011534658.1:p.Gly219=
XM_011536357.1:c.604G=	XP_011534659.1:p.Gly202=
XM_011536358.1:c.436G=	XP_011534660.1:p.Gly146=
XM_011536357.2:c.604G=	XP_011534659.1:p.Gly202=
XM_011536358.2:c.436G=	XP_011534660.1:p.Gly146=
XM_017020929.2:c.436G=	XP_016876418.1:p.Gly146=
NM_001384158.1:c.727G=	NP_001371087.1:p.Gly243=
NM_001384159.1:c.655G=	NP_001371088.1:p.Gly219=
NM_001384160.1:c.604G=	NP_001371089.1:p.Gly202=
NM_001384161.1:c.436G=	NP_001371090.1:p.Gly146=
NM_001384162.1:c.436G=	NP_001371091.1:p.Gly146=
NM_006329.4:c.604G= MANE Select	NP_006320.2:p.Gly202=