Canonical Allele Identifier: CA392325793
Community Standard Title: NM_000138.5(FBN1):c.7579G>C (p.Glu2527Gln)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48421678C>G , CM000677.2:g.48421678C>G GRCh38
NC_000015.9:g.48713875C>G , CM000677.1:g.48713875C>G GRCh37
NC_000015.8:g.46501167C>G NCBI36
NG_008805.2:g.229111G>C , LRG_778:g.229111G>C

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.7579G>C MANE Select NP_000129.3:p.Glu2527Gln
ENST00000316623.10:c.7579G>C MANE Select ENSP00000325527.5:p.Glu2527Gln
NM_000138.4:c.7579G>C , LRG_778t1:c.7579G>C NP_000129.3:p.Glu2527Gln
ENST00000316623.9:c.7579G>C ENSP00000325527.5:p.Glu2527Gln
ENST00000559133.5:c.2948G>C
ENST00000559133.6:c.*387G>C ENSP00000453958.2:n.*387G>C
ENST00000674301.1:c.2745G>C ENSP00000501333.1:n.2745G>C
ENST00000674301.2:c.*1092G>C ENSP00000501333.2:n.*1092G>C
ENST00000682170.1:n.1760G>C
ENST00000682767.1:n.876G>C