Canonical Allele Identifier: CA2175463175
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48421511C= , CM000677.2:g.48421511C= GRCh38
NC_000015.9:g.48713708C= , CM000677.1:g.48713708C= GRCh37
NC_000015.8:g.46501000C= NCBI36
NG_008805.2:g.229278G= , LRG_778:g.229278G=

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.*507+47G= ENSP00000453958.2:n.*507+47G=
ENST00000674301.2:c.*1212+47G= ENSP00000501333.2:n.*1212+47G=
ENST00000682170.1:n.1880+47G=
ENST00000682767.1:n.996+47G=
ENST00000316623.10:c.7699+47G= MANE Select ENSP00000325527.5:n.7699+47G=
ENST00000674301.1:c.2865+47G= ENSP00000501333.1:n.2865+47G=
ENST00000316623.9:c.7699+47G= ENSP00000325527.5:n.7699+47G=
ENST00000559133.5:c.3068+47G=
NM_000138.4:c.7699+47G= , LRG_778t1:c.7699+47G= NP_000129.3:n.7699+47G=
NM_000138.5:c.7699+47G= MANE Select NP_000129.3:n.7699+47G=