Canonical Allele Identifier: CA2175492023
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48472576G= , CM000677.2:g.48472576G= GRCh38
NC_000015.9:g.48764773G= , CM000677.1:g.48764773G= GRCh37
NC_000015.8:g.46552065G= NCBI36
NG_008805.2:g.178213C= , LRG_778:g.178213C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4311C= ENSP00000453958.2:p.Pro1437=
ENST00000674301.2:c.4311C= ENSP00000501333.2:p.Pro1437=
ENST00000683268.1:n.278C=
ENST00000684448.1:n.2985C=
ENST00000316623.10:c.4311C= MANE Select ENSP00000325527.5:p.Pro1437=
ENST00000316623.9:c.4311C= ENSP00000325527.5:p.Pro1437=
ENST00000537463.6:c.*74C= ENSP00000440294.2:n.*74C=
NM_000138.4:c.4311C= , LRG_778t1:c.4311C= NP_000129.3:p.Pro1437=
NM_000138.5:c.4311C= MANE Select NP_000129.3:p.Pro1437=