Canonical Allele Identifier: CA2175531369

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48513528C= , CM000677.2:g.48513528C=	GRCh38
NC_000015.9:g.48805725C= , CM000677.1:g.48805725C=	GRCh37
NC_000015.8:g.46593017C=	NCBI36
NG_008805.2:g.137261G= , LRG_778:g.137261G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000559133.6:c.1588+21G=	ENSP00000453958.2:n.1588+21G=
ENST00000674301.2:c.1588+21G=	ENSP00000501333.2:n.1588+21G=
ENST00000684448.1:n.262+21G=
ENST00000316623.10:c.1588+21G= MANE Select	ENSP00000325527.5:n.1588+21G=
ENST00000316623.9:c.1588+21G=	ENSP00000325527.5:n.1588+21G=
ENST00000537463.6:c.636+24183G=	ENSP00000440294.2:n.636+24183G=
NM_000138.4:c.1588+21G= , LRG_778t1:c.1588+21G=	NP_000129.3:n.1588+21G=
NM_000138.5:c.1588+21G= MANE Select	NP_000129.3:n.1588+21G=