Canonical Allele Identifier: CA2175463842
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48421693G= , CM000677.2:g.48421693G= GRCh38
NC_000015.9:g.48713890G= , CM000677.1:g.48713890G= GRCh37
NC_000015.8:g.46501182G= NCBI36
NG_008805.2:g.229096C= , LRG_778:g.229096C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*379-7C= ENSP00000453958.2:n.*379-7C=
ENST00000674301.2:c.*1084-7C= ENSP00000501333.2:n.*1084-7C=
ENST00000682170.1:n.1752-7C=
ENST00000682767.1:n.868-7C=
ENST00000316623.10:c.7571-7C= MANE Select ENSP00000325527.5:n.7571-7C=
ENST00000674301.1:c.2737-7C= ENSP00000501333.1:n.2737-7C=
ENST00000316623.9:c.7571-7C= ENSP00000325527.5:n.7571-7C=
ENST00000559133.5:c.2940-7C=
NM_000138.4:c.7571-7C= , LRG_778t1:c.7571-7C= NP_000129.3:n.7571-7C=
NM_000138.5:c.7571-7C= MANE Select NP_000129.3:n.7571-7C=