Canonical Allele Identifier: CA392329915
Community Standard Title: NM_000138.5(FBN1):c.7088G>T (p.Cys2363Phe)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48427683C>A , CM000677.2:g.48427683C>A GRCh38
NC_000015.9:g.48719880C>A , CM000677.1:g.48719880C>A GRCh37
NC_000015.8:g.46507172C>A NCBI36
NG_008805.2:g.223106G>T , LRG_778:g.223106G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.7088G>T MANE Select NP_000129.3:p.Cys2363Phe
ENST00000316623.10:c.7088G>T MANE Select ENSP00000325527.5:p.Cys2363Phe
NM_000138.4:c.7088G>T , LRG_778t1:c.7088G>T NP_000129.3:p.Cys2363Phe
ENST00000316623.9:c.7088G>T ENSP00000325527.5:p.Cys2363Phe
ENST00000559133.5:c.2457G>T
ENST00000559133.6:c.7150G>T ENSP00000453958.2:p.Ala2384Ser
ENST00000674301.1:c.2254G>T ENSP00000501333.1:n.2254G>T
ENST00000674301.2:c.*601G>T ENSP00000501333.2:n.*601G>T
ENST00000682170.1:n.1269G>T
ENST00000682767.1:n.385G>T