Canonical Allele Identifier: CA2155139634

Gene: FBLN5

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91877687G= , CM000676.2:g.91877687G=	GRCh38
NC_000014.8:g.92344031G= , CM000676.1:g.92344031G=	GRCh37
NC_000014.7:g.91413784G=	NCBI36
NG_008254.1:g.75016C= , LRG_364:g.75016C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557088.6:c.*956-5C=	ENSP00000451002.1:n.*956-5C=
ENST00000557570.2:c.822-5C=	ENSP00000450787.2:n.822-5C=
ENST00000706675.1:n.805-5C=
ENST00000706676.1:c.1164-5C=	ENSP00000516492.1:n.1164-5C=
ENST00000706677.1:c.990-5C=	ENSP00000516493.1:n.990-5C=
ENST00000706678.1:n.910-5C=
ENST00000706679.1:c.822-5C=	ENSP00000516494.1:n.822-5C=
ENST00000706680.1:c.*833-5C=	ENSP00000516495.1:n.*833-5C=
ENST00000706681.1:c.*729-5C=	ENSP00000516496.1:n.*729-5C=
ENST00000342058.9:c.990-5C= MANE Select	ENSP00000345008.4:n.990-5C=
ENST00000267620.14:c.1113-5C=	ENSP00000267620.10:n.1113-5C=
ENST00000342058.8:c.990-5C=	ENSP00000345008.4:n.990-5C=
ENST00000554121.2:n.116-5C=
ENST00000556154.5:c.1005-5C=	ENSP00000451982.1:n.1005-5C=
NM_006329.3:c.990-5C= , LRG_364t1:c.990-5C=	NP_006320.2:n.990-5C=
XM_005267267.3:c.1041-5C=	XP_005267324.1:n.1041-5C=
XM_011536356.1:c.1041-5C=	XP_011534658.1:n.1041-5C=
XM_011536357.1:c.990-5C=	XP_011534659.1:n.990-5C=
XM_011536358.1:c.822-5C=	XP_011534660.1:n.822-5C=
XM_011536357.2:c.990-5C=	XP_011534659.1:n.990-5C=
XM_011536358.2:c.822-5C=	XP_011534660.1:n.822-5C=
XM_017020929.2:c.822-5C=	XP_016876418.1:n.822-5C=
NM_001384158.1:c.1113-5C=	NP_001371087.1:n.1113-5C=
NM_001384159.1:c.1041-5C=	NP_001371088.1:n.1041-5C=
NM_001384160.1:c.990-5C=	NP_001371089.1:n.990-5C=
NM_001384161.1:c.822-5C=	NP_001371090.1:n.822-5C=
NM_001384162.1:c.822-5C=	NP_001371091.1:n.822-5C=
NM_006329.4:c.990-5C= MANE Select	NP_006320.2:n.990-5C=