Canonical Allele Identifier: CA2592719884
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48445176_48445209dup , CM000677.2:g.48445176_48445209dup GRCh38
NC_000015.9:g.48737373_48737406dup , CM000677.1:g.48737373_48737406dup GRCh37
NC_000015.8:g.46524665_46524698dup NCBI36
NG_008805.2:g.205581_205614dup , LRG_778:g.205581_205614dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.5917+168_5917+201dup ENSP00000453958.2:n.5917+168_5917+201dup
ENST00000674301.2:c.5917+168_5917+201dup ENSP00000501333.2:n.5917+168_5917+201dup
ENST00000684448.1:n.4591+168_4591+201dup
ENST00000316623.10:c.5917+168_5917+201dup MANE Select ENSP00000325527.5:n.5917+168_5917+201dup
ENST00000674301.1:c.916+168_916+201dup ENSP00000501333.1:n.916+168_916+201dup
ENST00000316623.9:c.5917+168_5917+201dup ENSP00000325527.5:n.5917+168_5917+201dup
ENST00000537463.6:c.*1680+168_*1680+201dup ENSP00000440294.2:n.*1680+168_*1680+201dup
ENST00000559133.5:c.1224+168_1224+201dup
ENST00000560820.1:n.37+168_37+201dup
NM_000138.4:c.5917+168_5917+201dup , LRG_778t1:c.5917+168_5917+201dup NP_000129.3:n.5917+168_5917+201dup
NM_000138.5:c.5917+168_5917+201dup MANE Select NP_000129.3:n.5917+168_5917+201dup