Canonical Allele Identifier: CA2175513016
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48445125T= , CM000677.2:g.48445125T= GRCh38
NC_000015.9:g.48737322T= , CM000677.1:g.48737322T= GRCh37
NC_000015.8:g.46524614T= NCBI36
NG_008805.2:g.205664A= , LRG_778:g.205664A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.5917+251A= ENSP00000453958.2:n.5917+251A=
ENST00000674301.2:c.5917+251A= ENSP00000501333.2:n.5917+251A=
ENST00000684448.1:n.4591+251A=
ENST00000316623.10:c.5917+251A= MANE Select ENSP00000325527.5:n.5917+251A=
ENST00000674301.1:c.916+251A= ENSP00000501333.1:n.916+251A=
ENST00000316623.9:c.5917+251A= ENSP00000325527.5:n.5917+251A=
ENST00000537463.6:c.*1680+251A= ENSP00000440294.2:n.*1680+251A=
ENST00000559133.5:c.1224+251A=
ENST00000560820.1:n.37+251A=
NM_000138.4:c.5917+251A= , LRG_778t1:c.5917+251A= NP_000129.3:n.5917+251A=
NM_000138.5:c.5917+251A= MANE Select NP_000129.3:n.5917+251A=