Canonical Allele Identifier: CA2175463232
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48421543G= , CM000677.2:g.48421543G= GRCh38
NC_000015.9:g.48713740G= , CM000677.1:g.48713740G= GRCh37
NC_000015.8:g.46501032G= NCBI36
NG_008805.2:g.229246C= , LRG_778:g.229246C=

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.*507+15C= ENSP00000453958.2:n.*507+15C=
ENST00000674301.2:c.*1212+15C= ENSP00000501333.2:n.*1212+15C=
ENST00000682170.1:n.1880+15C=
ENST00000682767.1:n.996+15C=
ENST00000316623.10:c.7699+15C= MANE Select ENSP00000325527.5:n.7699+15C=
ENST00000674301.1:c.2865+15C= ENSP00000501333.1:n.2865+15C=
ENST00000316623.9:c.7699+15C= ENSP00000325527.5:n.7699+15C=
ENST00000559133.5:c.3068+15C=
NM_000138.4:c.7699+15C= , LRG_778t1:c.7699+15C= NP_000129.3:n.7699+15C=
NM_000138.5:c.7699+15C= MANE Select NP_000129.3:n.7699+15C=