Canonical Allele Identifier: CA392329368
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48489962C>T , CM000677.2:g.48489962C>T GRCh38
NC_000015.9:g.48782159C>T , CM000677.1:g.48782159C>T GRCh37
NC_000015.8:g.46569451C>T NCBI36
NG_008805.2:g.160827G>A , LRG_778:g.160827G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.2971G>A ENSP00000453958.2:p.Glu991Lys
ENST00000674301.2:c.2971G>A ENSP00000501333.2:p.Glu991Lys
ENST00000684448.1:n.1645G>A
ENST00000316623.10:c.2971G>A MANE Select ENSP00000325527.5:p.Glu991Lys
ENST00000316623.9:c.2971G>A ENSP00000325527.5:p.Glu991Lys
ENST00000537463.6:c.637-15312G>A ENSP00000440294.2:n.637-15312G>A
NM_000138.4:c.2971G>A , LRG_778t1:c.2971G>A NP_000129.3:p.Glu991Lys
NM_000138.5:c.2971G>A MANE Select NP_000129.3:p.Glu991Lys