Canonical Allele Identifier: CA2628334909
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48494114dup , CM000677.2:g.48494114dup GRCh38
NC_000015.9:g.48786311dup , CM000677.1:g.48786311dup GRCh37
NC_000015.8:g.46573603dup NCBI36
NG_008805.2:g.156675dup , LRG_778:g.156675dup

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.2728+90dup ENSP00000453958.2:n.2728+90dup
ENST00000674301.2:c.2728+90dup ENSP00000501333.2:n.2728+90dup
ENST00000684448.1:n.1402+90dup
ENST00000316623.10:c.2728+90dup MANE Select ENSP00000325527.5:n.2728+90dup
ENST00000316623.9:c.2728+90dup ENSP00000325527.5:n.2728+90dup
ENST00000537463.6:c.637-19464dup ENSP00000440294.2:n.637-19464dup
NM_000138.4:c.2728+90dup , LRG_778t1:c.2728+90dup NP_000129.3:n.2728+90dup
NM_000138.5:c.2728+90dup MANE Select NP_000129.3:n.2728+90dup