Canonical Allele Identifier: CA617836983
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs931622804

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48445135_48445136dup , CM000677.2:g.48445135_48445136dup GRCh38
NC_000015.9:g.48737332_48737333dup , CM000677.1:g.48737332_48737333dup GRCh37
NC_000015.8:g.46524624_46524625dup NCBI36
NG_008805.2:g.205664_205665dup , LRG_778:g.205664_205665dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.5917+251_5917+252dup ENSP00000453958.2:n.5917+251_5917+252dup
ENST00000674301.2:c.5917+251_5917+252dup ENSP00000501333.2:n.5917+251_5917+252dup
ENST00000684448.1:n.4591+251_4591+252dup
ENST00000316623.10:c.5917+251_5917+252dup MANE Select ENSP00000325527.5:n.5917+251_5917+252dup
ENST00000674301.1:c.916+251_916+252dup ENSP00000501333.1:n.916+251_916+252dup
ENST00000316623.9:c.5917+251_5917+252dup ENSP00000325527.5:n.5917+251_5917+252dup
ENST00000537463.6:c.*1680+251_*1680+252dup ENSP00000440294.2:n.*1680+251_*1680+252dup
ENST00000559133.5:c.1224+251_1224+252dup
ENST00000560820.1:n.37+251_37+252dup
NM_000138.4:c.5917+251_5917+252dup , LRG_778t1:c.5917+251_5917+252dup NP_000129.3:n.5917+251_5917+252dup
NM_000138.5:c.5917+251_5917+252dup MANE Select NP_000129.3:n.5917+251_5917+252dup