Canonical Allele Identifier: CA392339804
Community Standard Title: NM_000138.5(FBN1):c.5965T>G (p.Cys1989Gly)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48444613A>C , CM000677.2:g.48444613A>C GRCh38
NC_000015.9:g.48736810A>C , CM000677.1:g.48736810A>C GRCh37
NC_000015.8:g.46524102A>C NCBI36
NG_008805.2:g.206176T>G , LRG_778:g.206176T>G

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.5965T>G MANE Select NP_000129.3:p.Cys1989Gly
ENST00000316623.10:c.5965T>G MANE Select ENSP00000325527.5:p.Cys1989Gly
NM_000138.4:c.5965T>G , LRG_778t1:c.5965T>G NP_000129.3:p.Cys1989Gly
ENST00000316623.9:c.5965T>G ENSP00000325527.5:p.Cys1989Gly
ENST00000537463.6:c.*1728T>G ENSP00000440294.2:n.*1728T>G
ENST00000559133.5:c.1272T>G
ENST00000559133.6:c.5965T>G ENSP00000453958.2:p.Cys1989Gly
ENST00000560820.1:n.85T>G
ENST00000674301.1:c.964T>G ENSP00000501333.1:p.Cys322Gly
ENST00000674301.2:c.5965T>G ENSP00000501333.2:p.Cys1989Gly
ENST00000684448.1:n.4639T>G