Canonical Allele Identifier: CA2175465009

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48422202G= , CM000677.2:g.48422202G=	GRCh38
NC_000015.9:g.48714399G= , CM000677.1:g.48714399G=	GRCh37
NC_000015.8:g.46501691G=	NCBI36
NG_008805.2:g.228587C= , LRG_778:g.228587C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*262-134C=	ENSP00000453958.2:n.*262-134C=
ENST00000674301.2:c.*967-134C=	ENSP00000501333.2:n.*967-134C=
ENST00000682170.1:n.1635-134C=
ENST00000682767.1:n.751-134C=
ENST00000316623.10:c.7454-134C= MANE Select	ENSP00000325527.5:n.7454-134C=
ENST00000674301.1:c.2620-134C=	ENSP00000501333.1:n.2620-134C=
ENST00000316623.9:c.7454-134C=	ENSP00000325527.5:n.7454-134C=
ENST00000559133.5:c.2823-134C=
NM_000138.4:c.7454-134C= , LRG_778t1:c.7454-134C=	NP_000129.3:n.7454-134C=
NM_000138.5:c.7454-134C= MANE Select	NP_000129.3:n.7454-134C=