Canonical Allele Identifier: CA2175511934
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48485451_48485454delinsCAGA , CM000677.2:g.48485451_48485454delinsCAGA GRCh38
NC_000015.9:g.48777648_48777651delinsCAGA , CM000677.1:g.48777648_48777651delinsCAGA GRCh37
NC_000015.8:g.46564940_46564943delinsCAGA NCBI36
NG_008805.2:g.165335_165338delinsTCTG , LRG_778:g.165335_165338delinsTCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.3632_3635delinsTCTG ENSP00000453958.2:p.Phe1211=
ENST00000674301.2:c.3632_3635delinsTCTG ENSP00000501333.2:p.Phe1211=
ENST00000684448.1:n.2306_2309delinsTCTG
ENST00000316623.10:c.3632_3635delinsTCTG MANE Select ENSP00000325527.5:p.Phe1211=
ENST00000316623.9:c.3632_3635delinsTCTG ENSP00000325527.5:p.Phe1211=
ENST00000537463.6:c.637-10804_637-10801delinsTCTG ENSP00000440294.2:n.637-10804_637-10801delinsTCTG
NM_000138.4:c.3632_3635delinsTCTG , LRG_778t1:c.3632_3635delinsTCTG NP_000129.3:p.Phe1211=
NM_000138.5:c.3632_3635delinsTCTG MANE Select NP_000129.3:p.Phe1211=