Canonical Allele Identifier: CA2175513276
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs2043145507

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48445162_48445174dup , CM000677.2:g.48445162_48445174dup GRCh38
NC_000015.9:g.48737359_48737371dup , CM000677.1:g.48737359_48737371dup GRCh37
NC_000015.8:g.46524651_46524663dup NCBI36
NG_008805.2:g.205615_205627dup , LRG_778:g.205615_205627dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.5917+202_5917+214dup ENSP00000453958.2:n.5917+202_5917+214dup
ENST00000674301.2:c.5917+202_5917+214dup ENSP00000501333.2:n.5917+202_5917+214dup
ENST00000684448.1:n.4591+202_4591+214dup
ENST00000316623.10:c.5917+202_5917+214dup MANE Select ENSP00000325527.5:n.5917+202_5917+214dup
ENST00000674301.1:c.916+202_916+214dup ENSP00000501333.1:n.916+202_916+214dup
ENST00000316623.9:c.5917+202_5917+214dup ENSP00000325527.5:n.5917+202_5917+214dup
ENST00000537463.6:c.*1680+202_*1680+214dup ENSP00000440294.2:n.*1680+202_*1680+214dup
ENST00000559133.5:c.1224+202_1224+214dup
ENST00000560820.1:n.37+202_37+214dup
NM_000138.4:c.5917+202_5917+214dup , LRG_778t1:c.5917+202_5917+214dup NP_000129.3:n.5917+202_5917+214dup
NM_000138.5:c.5917+202_5917+214dup MANE Select NP_000129.3:n.5917+202_5917+214dup