Canonical Allele Identifier: CA2175529894
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48510123_48510134delinsGCGTCCATTATT , CM000677.2:g.48510123_48510134delinsGCGTCCATTATT GRCh38
NC_000015.9:g.48802320_48802331delinsGCGTCCATTATT , CM000677.1:g.48802320_48802331delinsGCGTCCATTATT GRCh37
NC_000015.8:g.46589612_46589623delinsGCGTCCATTATT NCBI36
NG_008805.2:g.140655_140666delinsAATAATGGACGC , LRG_778:g.140655_140666delinsAATAATGGACGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.1624_1635delinsAATAATGGACGC ENSP00000453958.2:p.Asn542=
ENST00000674301.2:c.1624_1635delinsAATAATGGACGC ENSP00000501333.2:p.Asn542=
ENST00000684448.1:n.298_309delinsAATAATGGACGC
ENST00000316623.10:c.1624_1635delinsAATAATGGACGC MANE Select ENSP00000325527.5:p.Asn542=
ENST00000316623.9:c.1624_1635delinsAATAATGGACGC ENSP00000325527.5:p.Asn542=
ENST00000537463.6:c.636+27577_636+27588delinsAATAATGGACGC ENSP00000440294.2:n.636+27577_636+27588delinsAATAATGGACGC
NM_000138.4:c.1624_1635delinsAATAATGGACGC , LRG_778t1:c.1624_1635delinsAATAATGGACGC NP_000129.3:p.Asn542=
NM_000138.5:c.1624_1635delinsAATAATGGACGC MANE Select NP_000129.3:p.Asn542=