Canonical Allele Identifier: CA392322967

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48415632C>G , CM000677.2:g.48415632C>G	GRCh38
NC_000015.9:g.48707829C>G , CM000677.1:g.48707829C>G	GRCh37
NC_000015.8:g.46495121C>G	NCBI36
NG_008805.2:g.235157G>C , LRG_778:g.235157G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000138.5:c.7955G>C MANE Select	NP_000129.3:p.Cys2652Ser
ENST00000316623.10:c.7955G>C MANE Select	ENSP00000325527.5:p.Cys2652Ser
NM_000138.4:c.7955G>C , LRG_778t1:c.7955G>C	NP_000129.3:p.Cys2652Ser
ENST00000316623.9:c.7955G>C	ENSP00000325527.5:p.Cys2652Ser
ENST00000559133.5:c.3324G>C
ENST00000559133.6:c.*763G>C	ENSP00000453958.2:n.*763G>C
ENST00000561429.1:n.210G>C
ENST00000674301.1:c.3121G>C	ENSP00000501333.1:n.3121G>C
ENST00000674301.2:c.*1468G>C	ENSP00000501333.2:n.*1468G>C
ENST00000682158.1:n.1336G>C
ENST00000682170.1:n.2136G>C
ENST00000682767.1:n.1252G>C