Canonical Allele Identifier: CA2841790657
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48441638dup , CM000677.2:g.48441638dup GRCh38
NC_000015.9:g.48733835dup , CM000677.1:g.48733835dup GRCh37
NC_000015.8:g.46521127dup NCBI36
NG_008805.2:g.209151dup , LRG_778:g.209151dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.6163+83dup ENSP00000453958.2:n.6163+83dup
ENST00000674301.2:c.6163+83dup ENSP00000501333.2:n.6163+83dup
ENST00000316623.10:c.6163+83dup MANE Select ENSP00000325527.5:n.6163+83dup
ENST00000674301.1:c.1162+83dup ENSP00000501333.1:n.1162+83dup
ENST00000316623.9:c.6163+83dup ENSP00000325527.5:n.6163+83dup
ENST00000537463.6:c.*1926+83dup ENSP00000440294.2:n.*1926+83dup
ENST00000559133.5:c.1470+83dup
ENST00000560820.1:n.283+83dup
NM_000138.4:c.6163+83dup , LRG_778t1:c.6163+83dup NP_000129.3:n.6163+83dup
NM_000138.5:c.6163+83dup MANE Select NP_000129.3:n.6163+83dup