Canonical Allele Identifier: CA2175513088
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48445140A= , CM000677.2:g.48445140A= GRCh38
NC_000015.9:g.48737337A= , CM000677.1:g.48737337A= GRCh37
NC_000015.8:g.46524629A= NCBI36
NG_008805.2:g.205649T= , LRG_778:g.205649T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.5917+236T= ENSP00000453958.2:n.5917+236T=
ENST00000674301.2:c.5917+236T= ENSP00000501333.2:n.5917+236T=
ENST00000684448.1:n.4591+236T=
ENST00000316623.10:c.5917+236T= MANE Select ENSP00000325527.5:n.5917+236T=
ENST00000674301.1:c.916+236T= ENSP00000501333.1:n.916+236T=
ENST00000316623.9:c.5917+236T= ENSP00000325527.5:n.5917+236T=
ENST00000537463.6:c.*1680+236T= ENSP00000440294.2:n.*1680+236T=
ENST00000559133.5:c.1224+236T=
ENST00000560820.1:n.37+236T=
NM_000138.4:c.5917+236T= , LRG_778t1:c.5917+236T= NP_000129.3:n.5917+236T=
NM_000138.5:c.5917+236T= MANE Select NP_000129.3:n.5917+236T=