Canonical Allele Identifier: CA2175512702

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48444962T= , CM000677.2:g.48444962T=	GRCh38
NC_000015.9:g.48737159T= , CM000677.1:g.48737159T=	GRCh37
NC_000015.8:g.46524451T=	NCBI36
NG_008805.2:g.205827A= , LRG_778:g.205827A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.5918-302A=	ENSP00000453958.2:n.5918-302A=
ENST00000674301.2:c.5918-302A=	ENSP00000501333.2:n.5918-302A=
ENST00000684448.1:n.4592-302A=
ENST00000316623.10:c.5918-302A= MANE Select	ENSP00000325527.5:n.5918-302A=
ENST00000674301.1:c.917-302A=	ENSP00000501333.1:n.917-302A=
ENST00000316623.9:c.5918-302A=	ENSP00000325527.5:n.5918-302A=
ENST00000537463.6:c.*1681-302A=	ENSP00000440294.2:n.*1681-302A=
ENST00000559133.5:c.1225-302A=
ENST00000560820.1:n.38-302A=
NM_000138.4:c.5918-302A= , LRG_778t1:c.5918-302A=	NP_000129.3:n.5918-302A=
NM_000138.5:c.5918-302A= MANE Select	NP_000129.3:n.5918-302A=