Canonical Allele Identifier: CA392324395
Community Standard Title: NM_000138.5(FBN1):c.7817T>A (p.Val2606Asp)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48420689A>T , CM000677.2:g.48420689A>T GRCh38
NC_000015.9:g.48712886A>T , CM000677.1:g.48712886A>T GRCh37
NC_000015.8:g.46500178A>T NCBI36
NG_008805.2:g.230100T>A , LRG_778:g.230100T>A

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.7817T>A MANE Select NP_000129.3:p.Val2606Asp
ENST00000316623.10:c.7817T>A MANE Select ENSP00000325527.5:p.Val2606Asp
NM_000138.4:c.7817T>A , LRG_778t1:c.7817T>A NP_000129.3:p.Val2606Asp
ENST00000316623.9:c.7817T>A ENSP00000325527.5:p.Val2606Asp
ENST00000559133.5:c.3186T>A
ENST00000559133.6:c.*625T>A ENSP00000453958.2:n.*625T>A
ENST00000674301.1:c.2983T>A ENSP00000501333.1:n.2983T>A
ENST00000674301.2:c.*1330T>A ENSP00000501333.2:n.*1330T>A
ENST00000682170.1:n.1998T>A
ENST00000682767.1:n.1114T>A