Canonical Allele Identifier: CA2575716558
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48412478C>T , CM000677.2:g.48412478C>T GRCh38
NC_000015.9:g.48704675C>T , CM000677.1:g.48704675C>T GRCh37
NC_000015.8:g.46491967C>T NCBI36
NG_008805.2:g.238311G>A , LRG_778:g.238311G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*1034+91G>A ENSP00000453958.2:n.*1034+91G>A
ENST00000674301.2:c.*1739+91G>A ENSP00000501333.2:n.*1739+91G>A
ENST00000682158.1:n.1607+91G>A
ENST00000682170.1:n.2407+91G>A
ENST00000682767.1:n.1523+91G>A
ENST00000316623.10:c.8226+91G>A MANE Select ENSP00000325527.5:n.8226+91G>A
ENST00000674301.1:c.3392+91G>A ENSP00000501333.1:n.3392+91G>A
ENST00000316623.9:c.8226+91G>A ENSP00000325527.5:n.8226+91G>A
ENST00000559133.5:c.3595+91G>A
ENST00000561429.1:n.481+91G>A
NM_000138.4:c.8226+91G>A , LRG_778t1:c.8226+91G>A NP_000129.3:n.8226+91G>A
NM_000138.5:c.8226+91G>A MANE Select NP_000129.3:n.8226+91G>A