Canonical Allele Identifier: CA392337283
Community Standard Title: NM_000138.5(FBN1):c.6180C>A (p.Tyr2060Ter)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48437901G>T , CM000677.2:g.48437901G>T GRCh38
NC_000015.9:g.48730098G>T , CM000677.1:g.48730098G>T GRCh37
NC_000015.8:g.46517390G>T NCBI36
NG_008805.2:g.212888C>A , LRG_778:g.212888C>A

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.6180C>A MANE Select NP_000129.3:p.Tyr2060Ter
ENST00000316623.10:c.6180C>A MANE Select ENSP00000325527.5:p.Tyr2060Ter
NM_000138.4:c.6180C>A , LRG_778t1:c.6180C>A NP_000129.3:p.Tyr2060Ter
ENST00000316623.9:c.6180C>A ENSP00000325527.5:p.Tyr2060Ter
ENST00000537463.6:c.*1943C>A ENSP00000440294.2:n.*1943C>A
ENST00000559133.5:c.1487C>A
ENST00000559133.6:c.6180C>A ENSP00000453958.2:p.Tyr2060Ter
ENST00000560820.1:n.300C>A
ENST00000674301.1:c.1179C>A ENSP00000501333.1:p.Tyr393Ter
ENST00000674301.2:c.6180C>A ENSP00000501333.2:p.Tyr2060Ter