Canonical Allele Identifier: CA2175493846

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48432824T= , CM000677.2:g.48432824T=	GRCh38
NC_000015.9:g.48725021T= , CM000677.1:g.48725021T=	GRCh37
NC_000015.8:g.46512313T=	NCBI36
NG_008805.2:g.217965A= , LRG_778:g.217965A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6739+42A=	ENSP00000453958.2:n.6739+42A=
ENST00000674301.2:c.*190+42A=	ENSP00000501333.2:n.*190+42A=
ENST00000682170.1:n.348+42A=
ENST00000316623.10:c.6739+42A= MANE Select	ENSP00000325527.5:n.6739+42A=
ENST00000674301.1:c.1843+42A=	ENSP00000501333.1:n.1843+42A=
ENST00000316623.9:c.6739+42A=	ENSP00000325527.5:n.6739+42A=
ENST00000537463.6:c.*2502+42A=	ENSP00000440294.2:n.*2502+42A=
ENST00000559133.5:c.2046+42A=
ENST00000560720.1:n.26+42A=
NM_000138.4:c.6739+42A= , LRG_778t1:c.6739+42A=	NP_000129.3:n.6739+42A=
NM_000138.5:c.6739+42A= MANE Select	NP_000129.3:n.6739+42A=