Canonical Allele Identifier: CA2175492474
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48425443T= , CM000677.2:g.48425443T= GRCh38
NC_000015.9:g.48717640T= , CM000677.1:g.48717640T= GRCh37
NC_000015.8:g.46504932T= NCBI36
NG_008805.2:g.225346A= , LRG_778:g.225346A=

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.*187A= ENSP00000453958.2:n.*187A=
ENST00000674301.2:c.*892A= ENSP00000501333.2:n.*892A=
ENST00000682170.1:n.1560A=
ENST00000682767.1:n.676A=
ENST00000316623.10:c.7379A= MANE Select ENSP00000325527.5:p.Lys2460=
ENST00000674301.1:c.2545A= ENSP00000501333.1:n.2545A=
ENST00000316623.9:c.7379A= ENSP00000325527.5:p.Lys2460=
ENST00000559133.5:c.2748A=
NM_000138.4:c.7379A= , LRG_778t1:c.7379A= NP_000129.3:p.Lys2460=
NM_000138.5:c.7379A= MANE Select NP_000129.3:p.Lys2460=