Canonical Allele Identifier: CA2628331407
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48428155dup , CM000677.2:g.48428155dup GRCh38
NC_000015.9:g.48720352dup , CM000677.1:g.48720352dup GRCh37
NC_000015.8:g.46507644dup NCBI36
NG_008805.2:g.222635dup , LRG_778:g.222635dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.6997+192dup ENSP00000453958.2:n.6997+192dup
ENST00000674301.2:c.*448+192dup ENSP00000501333.2:n.*448+192dup
ENST00000682170.1:n.798dup
ENST00000682767.1:n.232+192dup
ENST00000316623.10:c.6997+192dup MANE Select ENSP00000325527.5:n.6997+192dup
ENST00000674301.1:c.2101+192dup ENSP00000501333.1:n.2101+192dup
ENST00000316623.9:c.6997+192dup ENSP00000325527.5:n.6997+192dup
ENST00000559133.5:c.2304+192dup
ENST00000560720.1:n.476dup
NM_000138.4:c.6997+192dup , LRG_778t1:c.6997+192dup NP_000129.3:n.6997+192dup
NM_000138.5:c.6997+192dup MANE Select NP_000129.3:n.6997+192dup