Canonical Allele Identifier: CA2175465042
Gene: FBN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48422219G= , CM000677.2:g.48422219G= GRCh38
NC_000015.9:g.48714416G= , CM000677.1:g.48714416G= GRCh37
NC_000015.8:g.46501708G= NCBI36
NG_008805.2:g.228570C= , LRG_778:g.228570C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*262-151C= ENSP00000453958.2:n.*262-151C=
ENST00000674301.2:c.*967-151C= ENSP00000501333.2:n.*967-151C=
ENST00000682170.1:n.1635-151C=
ENST00000682767.1:n.751-151C=
ENST00000316623.10:c.7454-151C= MANE Select ENSP00000325527.5:n.7454-151C=
ENST00000674301.1:c.2620-151C= ENSP00000501333.1:n.2620-151C=
ENST00000316623.9:c.7454-151C= ENSP00000325527.5:n.7454-151C=
ENST00000559133.5:c.2823-151C=
NM_000138.4:c.7454-151C= , LRG_778t1:c.7454-151C= NP_000129.3:n.7454-151C=
NM_000138.5:c.7454-151C= MANE Select NP_000129.3:n.7454-151C=
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