Canonical Allele Identifier: CA2175509551
Community Standard Title: NM_000138.5(FBN1):c.5330G= (p.Cys1777=)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48456729C= , CM000677.2:g.48456729C= GRCh38
NC_000015.9:g.48748926C= , CM000677.1:g.48748926C= GRCh37
NC_000015.8:g.46536218C= NCBI36
NG_008805.2:g.194060G= , LRG_778:g.194060G=

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.5330G= MANE Select NP_000129.3:p.Cys1777=
ENST00000316623.10:c.5330G= MANE Select ENSP00000325527.5:p.Cys1777=
NM_000138.4:c.5330G= , LRG_778t1:c.5330G= NP_000129.3:p.Cys1777=
ENST00000316623.9:c.5330G= ENSP00000325527.5:p.Cys1777=
ENST00000537463.6:c.*1093G= ENSP00000440294.2:n.*1093G=
ENST00000559133.5:c.637G=
ENST00000559133.6:c.5330G= ENSP00000453958.2:p.Cys1777=
ENST00000674301.1:c.329G= ENSP00000501333.1:p.Cys110=
ENST00000674301.2:c.5330G= ENSP00000501333.2:p.Cys1777=
ENST00000684448.1:n.4004G=