Canonical Allele Identifier: CA2838256815
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48428315dup , CM000677.2:g.48428315dup GRCh38
NC_000015.9:g.48720512dup , CM000677.1:g.48720512dup GRCh37
NC_000015.8:g.46507804dup NCBI36
NG_008805.2:g.222475dup , LRG_778:g.222475dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.6997+32dup ENSP00000453958.2:n.6997+32dup
ENST00000674301.2:c.*448+32dup ENSP00000501333.2:n.*448+32dup
ENST00000682170.1:n.638dup
ENST00000682767.1:n.232+32dup
ENST00000316623.10:c.6997+32dup MANE Select ENSP00000325527.5:n.6997+32dup
ENST00000674301.1:c.2101+32dup ENSP00000501333.1:n.2101+32dup
ENST00000316623.9:c.6997+32dup ENSP00000325527.5:n.6997+32dup
ENST00000559133.5:c.2304+32dup
ENST00000560720.1:n.316dup
NM_000138.4:c.6997+32dup , LRG_778t1:c.6997+32dup NP_000129.3:n.6997+32dup
NM_000138.5:c.6997+32dup MANE Select NP_000129.3:n.6997+32dup