Canonical Allele Identifier: CA2175493247
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48445663A= , CM000677.2:g.48445663A= GRCh38
NC_000015.9:g.48737860A= , CM000677.1:g.48737860A= GRCh37
NC_000015.8:g.46525152A= NCBI36
NG_008805.2:g.205126T= , LRG_778:g.205126T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.5789-159T= ENSP00000453958.2:n.5789-159T=
ENST00000674301.2:c.5789-159T= ENSP00000501333.2:n.5789-159T=
ENST00000684448.1:n.4463-159T=
ENST00000316623.10:c.5789-159T= MANE Select ENSP00000325527.5:n.5789-159T=
ENST00000674301.1:c.788-159T= ENSP00000501333.1:n.788-159T=
ENST00000316623.9:c.5789-159T= ENSP00000325527.5:n.5789-159T=
ENST00000537463.6:c.*1552-159T= ENSP00000440294.2:n.*1552-159T=
ENST00000559133.5:c.1096-159T=
NM_000138.4:c.5789-159T= , LRG_778t1:c.5789-159T= NP_000129.3:n.5789-159T=
NM_000138.5:c.5789-159T= MANE Select NP_000129.3:n.5789-159T=