Canonical Allele Identifier: CA2575716569
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48412521G>A , CM000677.2:g.48412521G>A GRCh38
NC_000015.9:g.48704718G>A , CM000677.1:g.48704718G>A GRCh37
NC_000015.8:g.46492010G>A NCBI36
NG_008805.2:g.238268C>T , LRG_778:g.238268C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.*1034+48C>T ENSP00000453958.2:n.*1034+48C>T
ENST00000674301.2:c.*1739+48C>T ENSP00000501333.2:n.*1739+48C>T
ENST00000682158.1:n.1607+48C>T
ENST00000682170.1:n.2407+48C>T
ENST00000682767.1:n.1523+48C>T
ENST00000316623.10:c.8226+48C>T MANE Select ENSP00000325527.5:n.8226+48C>T
ENST00000674301.1:c.3392+48C>T ENSP00000501333.1:n.3392+48C>T
ENST00000316623.9:c.8226+48C>T ENSP00000325527.5:n.8226+48C>T
ENST00000559133.5:c.3595+48C>T
ENST00000561429.1:n.481+48C>T
NM_000138.4:c.8226+48C>T , LRG_778t1:c.8226+48C>T NP_000129.3:n.8226+48C>T
NM_000138.5:c.8226+48C>T MANE Select NP_000129.3:n.8226+48C>T