Canonical Allele Identifier: CA2175518396
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48468390_48468393delinsTGAA , CM000677.2:g.48468390_48468393delinsTGAA GRCh38
NC_000015.9:g.48760587_48760590delinsTGAA , CM000677.1:g.48760587_48760590delinsTGAA GRCh37
NC_000015.8:g.46547879_46547882delinsTGAA NCBI36
NG_008805.2:g.182396_182399delinsTTCA , LRG_778:g.182396_182399delinsTTCA

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.4582+19_4582+22delinsTTCA ENSP00000453958.2:n.4582+19_4582+22delins...
ENST00000674301.2:c.4582+19_4582+22delinsTTCA ENSP00000501333.2:n.4582+19_4582+22delins...
ENST00000684448.1:n.3256+19_3256+22delinsTTCA
ENST00000316623.10:c.4582+19_4582+22delinsTTCA MANE Select ENSP00000325527.5:n.4582+19_4582+22delins...
ENST00000316623.9:c.4582+19_4582+22delinsTTCA ENSP00000325527.5:n.4582+19_4582+22delins...
ENST00000537463.6:c.*345+19_*345+22delinsTTCA ENSP00000440294.2:n.*345+19_*345+22delins...
NM_000138.4:c.4582+19_4582+22delinsTTCA , LRG_778t1:c.4582+19_4582+22delinsTTCA NP_000129.3:n.4582+19_4582+22delinsTTCA
NM_000138.5:c.4582+19_4582+22delinsTTCA MANE Select NP_000129.3:n.4582+19_4582+22delinsTTCA