Canonical Allele Identifier: CA2175508480
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48441638_48441640delinsCAG , CM000677.2:g.48441638_48441640delinsCAG GRCh38
NC_000015.9:g.48733835_48733837delinsCAG , CM000677.1:g.48733835_48733837delinsCAG GRCh37
NC_000015.8:g.46521127_46521129delinsCAG NCBI36
NG_008805.2:g.209149_209151delinsCTG , LRG_778:g.209149_209151delinsCTG

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.6163+81_6163+83delinsCTG ENSP00000453958.2:n.6163+81_6163+83delins...
ENST00000674301.2:c.6163+81_6163+83delinsCTG ENSP00000501333.2:n.6163+81_6163+83delins...
ENST00000316623.10:c.6163+81_6163+83delinsCTG MANE Select ENSP00000325527.5:n.6163+81_6163+83delins...
ENST00000674301.1:c.1162+81_1162+83delinsCTG ENSP00000501333.1:n.1162+81_1162+83delins...
ENST00000316623.9:c.6163+81_6163+83delinsCTG ENSP00000325527.5:n.6163+81_6163+83delins...
ENST00000537463.6:c.*1926+81_*1926+83delinsCTG ENSP00000440294.2:n.*1926+81_*1926+83deli...
ENST00000559133.5:c.1470+81_1470+83delinsCTG
ENST00000560820.1:n.283+81_283+83delinsCTG
NM_000138.4:c.6163+81_6163+83delinsCTG , LRG_778t1:c.6163+81_6163+83delinsCTG NP_000129.3:n.6163+81_6163+83delinsCTG
NM_000138.5:c.6163+81_6163+83delinsCTG MANE Select NP_000129.3:n.6163+81_6163+83delinsCTG