Canonical Allele Identifier: CA392328626
Community Standard Title: NM_000138.5(FBN1):c.7279T>C (p.Cys2427Arg)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48425790A>G , CM000677.2:g.48425790A>G GRCh38
NC_000015.9:g.48717987A>G , CM000677.1:g.48717987A>G GRCh37
NC_000015.8:g.46505279A>G NCBI36
NG_008805.2:g.224999T>C , LRG_778:g.224999T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.7279T>C MANE Select NP_000129.3:p.Cys2427Arg
ENST00000316623.10:c.7279T>C MANE Select ENSP00000325527.5:p.Cys2427Arg
NM_000138.4:c.7279T>C , LRG_778t1:c.7279T>C NP_000129.3:p.Cys2427Arg
ENST00000316623.9:c.7279T>C ENSP00000325527.5:p.Cys2427Arg
ENST00000559133.5:c.2648T>C
ENST00000559133.6:c.*87T>C ENSP00000453958.2:n.*87T>C
ENST00000674301.1:c.2445T>C ENSP00000501333.1:n.2445T>C
ENST00000674301.2:c.*792T>C ENSP00000501333.2:n.*792T>C
ENST00000682170.1:n.1460T>C
ENST00000682767.1:n.576T>C