Canonical Allele Identifier: CA392330037
Community Standard Title: NM_000138.5(FBN1):c.7072G>T (p.Val2358Phe)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48427699C>A , CM000677.2:g.48427699C>A GRCh38
NC_000015.9:g.48719896C>A , CM000677.1:g.48719896C>A GRCh37
NC_000015.8:g.46507188C>A NCBI36
NG_008805.2:g.223090G>T , LRG_778:g.223090G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.7072G>T MANE Select NP_000129.3:p.Val2358Phe
ENST00000316623.10:c.7072G>T MANE Select ENSP00000325527.5:p.Val2358Phe
NM_000138.4:c.7072G>T , LRG_778t1:c.7072G>T NP_000129.3:p.Val2358Phe
ENST00000316623.9:c.7072G>T ENSP00000325527.5:p.Val2358Phe
ENST00000559133.5:c.2441G>T
ENST00000559133.6:c.7134G>T ENSP00000453958.2:p.Pro2378=
ENST00000674301.1:c.2238G>T ENSP00000501333.1:n.2238G>T
ENST00000674301.2:c.*585G>T ENSP00000501333.2:n.*585G>T
ENST00000682170.1:n.1253G>T
ENST00000682767.1:n.369G>T