Canonical Allele Identifier: CA2175495795
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48427490A= , CM000677.2:g.48427490A= GRCh38
NC_000015.9:g.48719687A= , CM000677.1:g.48719687A= GRCh37
NC_000015.8:g.46506979A= NCBI36
NG_008805.2:g.223299T= , LRG_778:g.223299T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*12+77T= ENSP00000453958.2:n.*12+77T=
ENST00000674301.2:c.*717+77T= ENSP00000501333.2:n.*717+77T=
ENST00000682170.1:n.1385+77T=
ENST00000682767.1:n.501+77T=
ENST00000316623.10:c.7204+77T= MANE Select ENSP00000325527.5:n.7204+77T=
ENST00000674301.1:c.2370+77T= ENSP00000501333.1:n.2370+77T=
ENST00000316623.9:c.7204+77T= ENSP00000325527.5:n.7204+77T=
ENST00000559133.5:c.2573+77T=
NM_000138.4:c.7204+77T= , LRG_778t1:c.7204+77T= NP_000129.3:n.7204+77T=
NM_000138.5:c.7204+77T= MANE Select NP_000129.3:n.7204+77T=