Canonical Allele Identifier: CA392332864
Community Standard Title: NM_000138.5(FBN1):c.6753T>G (p.Cys2251Trp)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48430789A>C , CM000677.2:g.48430789A>C GRCh38
NC_000015.9:g.48722986A>C , CM000677.1:g.48722986A>C GRCh37
NC_000015.8:g.46510278A>C NCBI36
NG_008805.2:g.220000T>G , LRG_778:g.220000T>G

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.6753T>G MANE Select NP_000129.3:p.Cys2251Trp
ENST00000316623.10:c.6753T>G MANE Select ENSP00000325527.5:p.Cys2251Trp
NM_000138.4:c.6753T>G , LRG_778t1:c.6753T>G NP_000129.3:p.Cys2251Trp
ENST00000316623.9:c.6753T>G ENSP00000325527.5:p.Cys2251Trp
ENST00000537463.6:c.*2516T>G ENSP00000440294.2:n.*2516T>G
ENST00000559133.5:c.2060T>G
ENST00000559133.6:c.6753T>G ENSP00000453958.2:p.Cys2251Trp
ENST00000560720.1:n.40T>G
ENST00000674301.1:c.1857T>G ENSP00000501333.1:n.1857T>G
ENST00000674301.2:c.*204T>G ENSP00000501333.2:n.*204T>G
ENST00000682170.1:n.362T>G