Canonical Allele Identifier: CA392323450
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48415759C>G , CM000677.2:g.48415759C>G GRCh38
NC_000015.9:g.48707956C>G , CM000677.1:g.48707956C>G GRCh37
NC_000015.8:g.46495248C>G NCBI36
NG_008805.2:g.235030G>C , LRG_778:g.235030G>C

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.7828G>C MANE Select NP_000129.3:p.Glu2610Gln
ENST00000316623.10:c.7828G>C MANE Select ENSP00000325527.5:p.Glu2610Gln
NM_000138.4:c.7828G>C , LRG_778t1:c.7828G>C NP_000129.3:p.Glu2610Gln
ENST00000316623.9:c.7828G>C ENSP00000325527.5:p.Glu2610Gln
ENST00000559133.5:c.3197G>C
ENST00000559133.6:c.*636G>C ENSP00000453958.2:n.*636G>C
ENST00000561429.1:n.83G>C
ENST00000674301.1:c.2994G>C ENSP00000501333.1:n.2994G>C
ENST00000674301.2:c.*1341G>C ENSP00000501333.2:n.*1341G>C
ENST00000682158.1:n.1209G>C
ENST00000682170.1:n.2009G>C
ENST00000682767.1:n.1125G>C