Canonical Allele Identifier: CA392334787
Community Standard Title: NM_000138.5(FBN1):c.6584G>T (p.Gly2195Val)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48434626C>A , CM000677.2:g.48434626C>A GRCh38
NC_000015.9:g.48726823C>A , CM000677.1:g.48726823C>A GRCh37
NC_000015.8:g.46514115C>A NCBI36
NG_008805.2:g.216163G>T , LRG_778:g.216163G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.6584G>T MANE Select NP_000129.3:p.Gly2195Val
ENST00000316623.10:c.6584G>T MANE Select ENSP00000325527.5:p.Gly2195Val
NM_000138.4:c.6584G>T , LRG_778t1:c.6584G>T NP_000129.3:p.Gly2195Val
ENST00000316623.9:c.6584G>T ENSP00000325527.5:p.Gly2195Val
ENST00000537463.6:c.*2347G>T ENSP00000440294.2:n.*2347G>T
ENST00000559133.5:c.1891G>T
ENST00000559133.6:c.6584G>T ENSP00000453958.2:p.Gly2195Val
ENST00000674301.1:c.1583G>T ENSP00000501333.1:p.Gly528Val
ENST00000674301.2:c.6584G>T ENSP00000501333.2:p.Gly2195Val
ENST00000682170.1:n.193G>T