Canonical Allele Identifier: CA392349174
Community Standard Title: NM_000138.5(FBN1):c.5158T>C (p.Cys1720Arg)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48463148A>G , CM000677.2:g.48463148A>G GRCh38
NC_000015.9:g.48755345A>G , CM000677.1:g.48755345A>G GRCh37
NC_000015.8:g.46542637A>G NCBI36
NG_008805.2:g.187641T>C , LRG_778:g.187641T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.5158T>C MANE Select NP_000129.3:p.Cys1720Arg
ENST00000316623.10:c.5158T>C MANE Select ENSP00000325527.5:p.Cys1720Arg
NM_000138.4:c.5158T>C , LRG_778t1:c.5158T>C NP_000129.3:p.Cys1720Arg
ENST00000316623.9:c.5158T>C ENSP00000325527.5:p.Cys1720Arg
ENST00000537463.6:c.*921T>C ENSP00000440294.2:n.*921T>C
ENST00000559133.5:c.465T>C
ENST00000559133.6:c.5158T>C ENSP00000453958.2:p.Cys1720Arg
ENST00000674301.1:c.157T>C ENSP00000501333.1:p.Cys53Arg
ENST00000674301.2:c.5158T>C ENSP00000501333.2:p.Cys1720Arg
ENST00000684448.1:n.3832T>C