Canonical Allele Identifier: CA2175486114
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48411044_48411045delinsGA , CM000677.2:g.48411044_48411045delinsGA GRCh38
NC_000015.9:g.48703241_48703242delinsGA , CM000677.1:g.48703241_48703242delinsGA GRCh37
NC_000015.8:g.46490533_46490534delinsGA NCBI36
NG_008805.2:g.239744_239745delinsTC , LRG_778:g.239744_239745delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.*1369_*1370delinsTC ENSP00000453958.2:n.*1369_*1370delinsTC
ENST00000682158.1:n.1942_1943delinsTC
ENST00000682170.1:n.2742_2743delinsTC
ENST00000682767.1:n.1858_1859delinsTC
ENST00000316623.10:c.8561_8562delinsTC MANE Select ENSP00000325527.5:p.Leu2854=
ENST00000316623.9:c.8561_8562delinsTC ENSP00000325527.5:p.Leu2854=
ENST00000559133.5:c.3930_3931delinsTC
NM_000138.4:c.8561_8562delinsTC , LRG_778t1:c.8561_8562delinsTC NP_000129.3:p.Leu2854=
NM_000138.5:c.8561_8562delinsTC MANE Select NP_000129.3:p.Leu2854=