Canonical Allele Identifier: CA2175502302
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48437030T= , CM000677.2:g.48437030T= GRCh38
NC_000015.9:g.48729227T= , CM000677.1:g.48729227T= GRCh37
NC_000015.8:g.46516519T= NCBI36
NG_008805.2:g.213759A= , LRG_778:g.213759A=

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.6427A= ENSP00000453958.2:p.Ile2143=
ENST00000674301.2:c.6427A= ENSP00000501333.2:p.Ile2143=
ENST00000682170.1:n.36A=
ENST00000316623.10:c.6427A= MANE Select ENSP00000325527.5:p.Ile2143=
ENST00000674301.1:c.1426A= ENSP00000501333.1:p.Ile476=
ENST00000316623.9:c.6427A= ENSP00000325527.5:p.Ile2143=
ENST00000537463.6:c.*2190A= ENSP00000440294.2:n.*2190A=
ENST00000559133.5:c.1734A=
NM_000138.4:c.6427A= , LRG_778t1:c.6427A= NP_000129.3:p.Ile2143=
NM_000138.5:c.6427A= MANE Select NP_000129.3:p.Ile2143=