Canonical Allele Identifier: CA269526987
Community Standard Title: NM_000138.5(FBN1):c.6180C>T (p.Tyr2060=)
Gene: FBN1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.6180C>T MANE Select NP_000129.3:p.Tyr2060=
ENST00000316623.10:c.6180C>T MANE Select ENSP00000325527.5:p.Tyr2060=
NM_000138.4:c.6180C>T , LRG_778t1:c.6180C>T NP_000129.3:p.Tyr2060=
ENST00000316623.9:c.6180C>T ENSP00000325527.5:p.Tyr2060=
ENST00000537463.6:c.*1943C>T ENSP00000440294.2:n.*1943C>T
ENST00000559133.5:c.1487C>T
ENST00000559133.6:c.6180C>T ENSP00000453958.2:p.Tyr2060=
ENST00000560820.1:n.300C>T
ENST00000674301.1:c.1179C>T ENSP00000501333.1:p.Tyr393=
ENST00000674301.2:c.6180C>T ENSP00000501333.2:p.Tyr2060=