Canonical Allele Identifier: CA392325065
Community Standard Title: NM_000138.5(FBN1):c.7663G>A (p.Gly2555Arg)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48421594C>T , CM000677.2:g.48421594C>T GRCh38
NC_000015.9:g.48713791C>T , CM000677.1:g.48713791C>T GRCh37
NC_000015.8:g.46501083C>T NCBI36
NG_008805.2:g.229195G>A , LRG_778:g.229195G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.7663G>A MANE Select NP_000129.3:p.Gly2555Arg
ENST00000316623.10:c.7663G>A MANE Select ENSP00000325527.5:p.Gly2555Arg
NM_000138.4:c.7663G>A , LRG_778t1:c.7663G>A NP_000129.3:p.Gly2555Arg
ENST00000316623.9:c.7663G>A ENSP00000325527.5:p.Gly2555Arg
ENST00000559133.5:c.3032G>A
ENST00000559133.6:c.*471G>A ENSP00000453958.2:n.*471G>A
ENST00000674301.1:c.2829G>A ENSP00000501333.1:n.2829G>A
ENST00000674301.2:c.*1176G>A ENSP00000501333.2:n.*1176G>A
ENST00000682170.1:n.1844G>A
ENST00000682767.1:n.960G>A