Canonical Allele Identifier: CA059621
Community Standard Title: NM_000138.5(FBN1):c.8098C>T (p.Pro2700Ser)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48412697G>A , CM000677.2:g.48412697G>A GRCh38
NC_000015.9:g.48704894G>A , CM000677.1:g.48704894G>A GRCh37
NC_000015.8:g.46492186G>A NCBI36
NG_008805.2:g.238092C>T , LRG_778:g.238092C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.8098C>T MANE Select NP_000129.3:p.Pro2700Ser
ENST00000316623.10:c.8098C>T MANE Select ENSP00000325527.5:p.Pro2700Ser
NM_000138.4:c.8098C>T , LRG_778t1:c.8098C>T NP_000129.3:p.Pro2700Ser
ENST00000316623.9:c.8098C>T ENSP00000325527.5:p.Pro2700Ser
ENST00000559133.5:c.3467C>T
ENST00000559133.6:c.*906C>T ENSP00000453958.2:n.*906C>T
ENST00000561429.1:n.353C>T
ENST00000674301.1:c.3264C>T ENSP00000501333.1:n.3264C>T
ENST00000674301.2:c.*1611C>T ENSP00000501333.2:n.*1611C>T
ENST00000682158.1:n.1479C>T
ENST00000682170.1:n.2279C>T
ENST00000682767.1:n.1395C>T