Canonical Allele Identifier: CA392341824
Community Standard Title: NM_000138.5(FBN1):c.5636G>A (p.Gly1879Asp)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48448803C>T , CM000677.2:g.48448803C>T GRCh38
NC_000015.9:g.48741000C>T , CM000677.1:g.48741000C>T GRCh37
NC_000015.8:g.46528292C>T NCBI36
NG_008805.2:g.201986G>A , LRG_778:g.201986G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.5636G>A MANE Select NP_000129.3:p.Gly1879Asp
ENST00000316623.10:c.5636G>A MANE Select ENSP00000325527.5:p.Gly1879Asp
NM_000138.4:c.5636G>A , LRG_778t1:c.5636G>A NP_000129.3:p.Gly1879Asp
ENST00000316623.9:c.5636G>A ENSP00000325527.5:p.Gly1879Asp
ENST00000537463.6:c.*1399G>A ENSP00000440294.2:n.*1399G>A
ENST00000559133.5:c.943G>A
ENST00000559133.6:c.5636G>A ENSP00000453958.2:p.Gly1879Asp
ENST00000674301.1:c.635G>A ENSP00000501333.1:p.Gly212Asp
ENST00000674301.2:c.5636G>A ENSP00000501333.2:p.Gly1879Asp
ENST00000684448.1:n.4310G>A