Canonical Allele Identifier: CA392328752
Community Standard Title: NM_000138.5(FBN1):c.7252T>C (p.Cys2418Arg)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48425817A>G , CM000677.2:g.48425817A>G GRCh38
NC_000015.9:g.48718014A>G , CM000677.1:g.48718014A>G GRCh37
NC_000015.8:g.46505306A>G NCBI36
NG_008805.2:g.224972T>C , LRG_778:g.224972T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.7252T>C MANE Select NP_000129.3:p.Cys2418Arg
ENST00000316623.10:c.7252T>C MANE Select ENSP00000325527.5:p.Cys2418Arg
NM_000138.4:c.7252T>C , LRG_778t1:c.7252T>C NP_000129.3:p.Cys2418Arg
ENST00000316623.9:c.7252T>C ENSP00000325527.5:p.Cys2418Arg
ENST00000559133.5:c.2621T>C
ENST00000559133.6:c.*60T>C ENSP00000453958.2:n.*60T>C
ENST00000674301.1:c.2418T>C ENSP00000501333.1:n.2418T>C
ENST00000674301.2:c.*765T>C ENSP00000501333.2:n.*765T>C
ENST00000682170.1:n.1433T>C
ENST00000682767.1:n.549T>C