Canonical Allele Identifier: CA2175496793

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48434562G= , CM000677.2:g.48434562G=	GRCh38
NC_000015.9:g.48726759G= , CM000677.1:g.48726759G=	GRCh37
NC_000015.8:g.46514051G=	NCBI36
NG_008805.2:g.216227C= , LRG_778:g.216227C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6616+32C=	ENSP00000453958.2:n.6616+32C=
ENST00000674301.2:c.6616+32C=	ENSP00000501333.2:n.6616+32C=
ENST00000682170.1:n.225+32C=
ENST00000316623.10:c.6616+32C= MANE Select	ENSP00000325527.5:n.6616+32C=
ENST00000674301.1:c.1615+32C=	ENSP00000501333.1:n.1615+32C=
ENST00000316623.9:c.6616+32C=	ENSP00000325527.5:n.6616+32C=
ENST00000537463.6:c.*2379+32C=	ENSP00000440294.2:n.*2379+32C=
ENST00000559133.5:c.1923+32C=
NM_000138.4:c.6616+32C= , LRG_778t1:c.6616+32C=	NP_000129.3:n.6616+32C=
NM_000138.5:c.6616+32C= MANE Select	NP_000129.3:n.6616+32C=