Canonical Allele Identifier: CA058149
Community Standard Title: NM_000138.5(FBN1):c.7231G>A (p.Asp2411Asn)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48425838C>T , CM000677.2:g.48425838C>T GRCh38
NC_000015.9:g.48718035C>T , CM000677.1:g.48718035C>T GRCh37
NC_000015.8:g.46505327C>T NCBI36
NG_008805.2:g.224951G>A , LRG_778:g.224951G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.7231G>A MANE Select NP_000129.3:p.Asp2411Asn
ENST00000316623.10:c.7231G>A MANE Select ENSP00000325527.5:p.Asp2411Asn
NM_000138.4:c.7231G>A , LRG_778t1:c.7231G>A NP_000129.3:p.Asp2411Asn
ENST00000316623.9:c.7231G>A ENSP00000325527.5:p.Asp2411Asn
ENST00000559133.5:c.2600G>A
ENST00000559133.6:c.*39G>A ENSP00000453958.2:n.*39G>A
ENST00000674301.1:c.2397G>A ENSP00000501333.1:n.2397G>A
ENST00000674301.2:c.*744G>A ENSP00000501333.2:n.*744G>A
ENST00000682170.1:n.1412G>A
ENST00000682767.1:n.528G>A