Canonical Allele Identifier: CA392320078
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48474287T>A , CM000677.2:g.48474287T>A GRCh38
NC_000015.9:g.48766484T>A , CM000677.1:g.48766484T>A GRCh37
NC_000015.8:g.46553776T>A NCBI36
NG_008805.2:g.176502A>T , LRG_778:g.176502A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4178A>T ENSP00000453958.2:p.Glu1393Val
ENST00000674301.2:c.4178A>T ENSP00000501333.2:p.Glu1393Val
ENST00000684448.1:n.2852A>T
ENST00000316623.10:c.4178A>T MANE Select ENSP00000325527.5:p.Glu1393Val
ENST00000316623.9:c.4178A>T ENSP00000325527.5:p.Glu1393Val
ENST00000537463.6:c.850A>T ENSP00000440294.2:p.Lys284Ter
NM_000138.4:c.4178A>T , LRG_778t1:c.4178A>T NP_000129.3:p.Glu1393Val
NM_000138.5:c.4178A>T MANE Select NP_000129.3:p.Glu1393Val