Canonical Allele Identifier: CA2175464003
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48421801T= , CM000677.2:g.48421801T= GRCh38
NC_000015.9:g.48713998T= , CM000677.1:g.48713998T= GRCh37
NC_000015.8:g.46501290T= NCBI36
NG_008805.2:g.228988A= , LRG_778:g.228988A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*379-115A= ENSP00000453958.2:n.*379-115A=
ENST00000674301.2:c.*1084-115A= ENSP00000501333.2:n.*1084-115A=
ENST00000682170.1:n.1752-115A=
ENST00000682767.1:n.868-115A=
ENST00000316623.10:c.7571-115A= MANE Select ENSP00000325527.5:n.7571-115A=
ENST00000674301.1:c.2737-115A= ENSP00000501333.1:n.2737-115A=
ENST00000316623.9:c.7571-115A= ENSP00000325527.5:n.7571-115A=
ENST00000559133.5:c.2940-115A=
NM_000138.4:c.7571-115A= , LRG_778t1:c.7571-115A= NP_000129.3:n.7571-115A=
NM_000138.5:c.7571-115A= MANE Select NP_000129.3:n.7571-115A=