Canonical Allele Identifier: CA2175464947
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48422158T= , CM000677.2:g.48422158T= GRCh38
NC_000015.9:g.48714355T= , CM000677.1:g.48714355T= GRCh37
NC_000015.8:g.46501647T= NCBI36
NG_008805.2:g.228631A= , LRG_778:g.228631A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*262-90A= ENSP00000453958.2:n.*262-90A=
ENST00000674301.2:c.*967-90A= ENSP00000501333.2:n.*967-90A=
ENST00000682170.1:n.1635-90A=
ENST00000682767.1:n.751-90A=
ENST00000316623.10:c.7454-90A= MANE Select ENSP00000325527.5:n.7454-90A=
ENST00000674301.1:c.2620-90A= ENSP00000501333.1:n.2620-90A=
ENST00000316623.9:c.7454-90A= ENSP00000325527.5:n.7454-90A=
ENST00000559133.5:c.2823-90A=
NM_000138.4:c.7454-90A= , LRG_778t1:c.7454-90A= NP_000129.3:n.7454-90A=
NM_000138.5:c.7454-90A= MANE Select NP_000129.3:n.7454-90A=