Canonical Allele Identifier: CA2628333506
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48468686_48468687del , CM000677.2:g.48468686_48468687del GRCh38
NC_000015.9:g.48760883_48760884del , CM000677.1:g.48760883_48760884del GRCh37
NC_000015.8:g.46548175_46548176del NCBI36
NG_008805.2:g.182105_182106del , LRG_778:g.182105_182106del

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4460-150_4460-149del ENSP00000453958.2:n.4460-150_4460-149del
ENST00000674301.2:c.4460-150_4460-149del ENSP00000501333.2:n.4460-150_4460-149del
ENST00000684448.1:n.3134-150_3134-149del
ENST00000316623.10:c.4460-150_4460-149del MANE Select ENSP00000325527.5:n.4460-150_4460-149del
ENST00000316623.9:c.4460-150_4460-149del ENSP00000325527.5:n.4460-150_4460-149del
ENST00000537463.6:c.*223-150_*223-149del ENSP00000440294.2:n.*223-150_*223-149del
NM_000138.4:c.4460-150_4460-149del , LRG_778t1:c.4460-150_4460-149del NP_000129.3:n.4460-150_4460-149del
NM_000138.5:c.4460-150_4460-149del MANE Select NP_000129.3:n.4460-150_4460-149del