Canonical Allele Identifier: CA392317785
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48472608A>T , CM000677.2:g.48472608A>T GRCh38
NC_000015.9:g.48764805A>T , CM000677.1:g.48764805A>T GRCh37
NC_000015.8:g.46552097A>T NCBI36
NG_008805.2:g.178181T>A , LRG_778:g.178181T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4279T>A ENSP00000453958.2:p.Tyr1427Asn
ENST00000674301.2:c.4279T>A ENSP00000501333.2:p.Tyr1427Asn
ENST00000683268.1:n.246T>A
ENST00000684448.1:n.2953T>A
ENST00000316623.10:c.4279T>A MANE Select ENSP00000325527.5:p.Tyr1427Asn
ENST00000316623.9:c.4279T>A ENSP00000325527.5:p.Tyr1427Asn
ENST00000537463.6:c.*42T>A ENSP00000440294.2:n.*42T>A
NM_000138.4:c.4279T>A , LRG_778t1:c.4279T>A NP_000129.3:p.Tyr1427Asn
NM_000138.5:c.4279T>A MANE Select NP_000129.3:p.Tyr1427Asn