Canonical Allele Identifier: CA2175515476
Community Standard Title: NM_000138.5(FBN1):c.5207G= (p.Cys1736=)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48463099C= , CM000677.2:g.48463099C= GRCh38
NC_000015.9:g.48755296C= , CM000677.1:g.48755296C= GRCh37
NC_000015.8:g.46542588C= NCBI36
NG_008805.2:g.187690G= , LRG_778:g.187690G=

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.5207G= MANE Select NP_000129.3:p.Cys1736=
ENST00000316623.10:c.5207G= MANE Select ENSP00000325527.5:p.Cys1736=
NM_000138.4:c.5207G= , LRG_778t1:c.5207G= NP_000129.3:p.Cys1736=
ENST00000316623.9:c.5207G= ENSP00000325527.5:p.Cys1736=
ENST00000537463.6:c.*970G= ENSP00000440294.2:n.*970G=
ENST00000559133.5:c.514G=
ENST00000559133.6:c.5207G= ENSP00000453958.2:p.Cys1736=
ENST00000674301.1:c.206G= ENSP00000501333.1:p.Cys69=
ENST00000674301.2:c.5207G= ENSP00000501333.2:p.Cys1736=
ENST00000684448.1:n.3881G=