Canonical Allele Identifier: CA392341306
Community Standard Title: NM_000138.5(FBN1):c.5714G>T (p.Cys1905Phe)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48446780C>A , CM000677.2:g.48446780C>A GRCh38
NC_000015.9:g.48738977C>A , CM000677.1:g.48738977C>A GRCh37
NC_000015.8:g.46526269C>A NCBI36
NG_008805.2:g.204009G>T , LRG_778:g.204009G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.5714G>T MANE Select NP_000129.3:p.Cys1905Phe
ENST00000316623.10:c.5714G>T MANE Select ENSP00000325527.5:p.Cys1905Phe
NM_000138.4:c.5714G>T , LRG_778t1:c.5714G>T NP_000129.3:p.Cys1905Phe
ENST00000316623.9:c.5714G>T ENSP00000325527.5:p.Cys1905Phe
ENST00000537463.6:c.*1477G>T ENSP00000440294.2:n.*1477G>T
ENST00000559133.5:c.1021G>T
ENST00000559133.6:c.5714G>T ENSP00000453958.2:p.Cys1905Phe
ENST00000674301.1:c.713G>T ENSP00000501333.1:p.Cys238Phe
ENST00000674301.2:c.5714G>T ENSP00000501333.2:p.Cys1905Phe
ENST00000684448.1:n.4388G>T