Canonical Allele Identifier: CA2575717179
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48472534_48472535del , CM000677.2:g.48472534_48472535del GRCh38
NC_000015.9:g.48764731_48764732del , CM000677.1:g.48764731_48764732del GRCh37
NC_000015.8:g.46552023_46552024del NCBI36
NG_008805.2:g.178254_178255del , LRG_778:g.178254_178255del

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4336+16_4336+17del ENSP00000453958.2:n.4336+16_4336+17del
ENST00000674301.2:c.4336+16_4336+17del ENSP00000501333.2:n.4336+16_4336+17del
ENST00000683268.1:n.303+16_303+17del
ENST00000684448.1:n.3010+16_3010+17del
ENST00000316623.10:c.4336+16_4336+17del MANE Select ENSP00000325527.5:n.4336+16_4336+17del
ENST00000316623.9:c.4336+16_4336+17del ENSP00000325527.5:n.4336+16_4336+17del
ENST00000537463.6:c.*99+16_*99+17del ENSP00000440294.2:n.*99+16_*99+17del
NM_000138.4:c.4336+16_4336+17del , LRG_778t1:c.4336+16_4336+17del NP_000129.3:n.4336+16_4336+17del
NM_000138.5:c.4336+16_4336+17del MANE Select NP_000129.3:n.4336+16_4336+17del