Canonical Allele Identifier: CA2175502796
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48430759T= , CM000677.2:g.48430759T= GRCh38
NC_000015.9:g.48722956T= , CM000677.1:g.48722956T= GRCh37
NC_000015.8:g.46510248T= NCBI36
NG_008805.2:g.220030A= , LRG_778:g.220030A=

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.6783A= ENSP00000453958.2:p.Lys2261=
ENST00000674301.2:c.*234A= ENSP00000501333.2:n.*234A=
ENST00000682170.1:n.392A=
ENST00000316623.10:c.6783A= MANE Select ENSP00000325527.5:p.Lys2261=
ENST00000674301.1:c.1887A= ENSP00000501333.1:n.1887A=
ENST00000316623.9:c.6783A= ENSP00000325527.5:p.Lys2261=
ENST00000559133.5:c.2090A=
ENST00000560720.1:n.70A=
NM_000138.4:c.6783A= , LRG_778t1:c.6783A= NP_000129.3:p.Lys2261=
NM_000138.5:c.6783A= MANE Select NP_000129.3:p.Lys2261=