Canonical Allele Identifier: CA2175512935
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48445109_48445123delinsTATATATATATACAC , CM000677.2:g.48445109_48445123delinsTATATATATATACAC GRCh38
NC_000015.9:g.48737306_48737320delinsTATATATATATACAC , CM000677.1:g.48737306_48737320delinsTATATATATATACAC GRCh37
NC_000015.8:g.46524598_46524612delinsTATATATATATACAC NCBI36
NG_008805.2:g.205666_205680delinsGTGTATATATATATA , LRG_778:g.205666_205680delinsGTGTATATATATATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.5917+253_5917+267delinsGTGTATATATATATA ENSP00000453958.2:n.5917+253_5917+267delinsGTGTATATATATATA
ENST00000674301.2:c.5917+253_5917+267delinsGTGTATATATATATA ENSP00000501333.2:n.5917+253_5917+267delinsGTGTATATATATATA
ENST00000684448.1:n.4591+253_4591+267delinsGTGTATATATATATA
ENST00000316623.10:c.5917+253_5917+267delinsGTGTATATATATATA MANE Select ENSP00000325527.5:n.5917+253_5917+267delinsGTGTATATATATATA
ENST00000674301.1:c.916+253_916+267delinsGTGTATATATATATA ENSP00000501333.1:n.916+253_916+267delinsGTGTATATATATATA
ENST00000316623.9:c.5917+253_5917+267delinsGTGTATATATATATA ENSP00000325527.5:n.5917+253_5917+267delinsGTGTATATATATATA
ENST00000537463.6:c.*1680+253_*1680+267delinsGTGTATATATATATA ENSP00000440294.2:n.*1680+253_*1680+267delinsGTGTATATATATATA
ENST00000559133.5:c.1224+253_1224+267delinsGTGTATATATATATA
ENST00000560820.1:n.37+253_37+267delinsGTGTATATATATATA
NM_000138.4:c.5917+253_5917+267delinsGTGTATATATATATA , LRG_778t1:c.5917+253_5917+267delinsGTGTATATATATATA NP_000129.3:n.5917+253_5917+267delinsGTGTATATATATATA
NM_000138.5:c.5917+253_5917+267delinsGTGTATATATATATA MANE Select NP_000129.3:n.5917+253_5917+267delinsGTGTATATATATATA