Canonical Allele Identifier: CA2628329850
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48422121_48422122insCTTCCCT , CM000677.2:g.48422121_48422122insCTTCCCT GRCh38
NC_000015.9:g.48714318_48714319insCTTCCCT , CM000677.1:g.48714318_48714319insCTTCCCT GRCh37
NC_000015.8:g.46501610_46501611insCTTCCCT NCBI36
NG_008805.2:g.228667_228668insAGGGAAG , LRG_778:g.228667_228668insAGGGAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*262-54_*262-53insAGGGAAG ENSP00000453958.2:n.*262-54_*262-53insAGGGAAG
ENST00000674301.2:c.*967-54_*967-53insAGGGAAG ENSP00000501333.2:n.*967-54_*967-53insAGGGAAG
ENST00000682170.1:n.1635-54_1635-53insAGGGAAG
ENST00000682767.1:n.751-54_751-53insAGGGAAG
ENST00000316623.10:c.7454-54_7454-53insAGGGAAG MANE Select ENSP00000325527.5:n.7454-54_7454-53insAGGGAAG
ENST00000674301.1:c.2620-54_2620-53insAGGGAAG ENSP00000501333.1:n.2620-54_2620-53insAGGGAAG
ENST00000316623.9:c.7454-54_7454-53insAGGGAAG ENSP00000325527.5:n.7454-54_7454-53insAGGGAAG
ENST00000559133.5:c.2823-54_2823-53insAGGGAAG
NM_000138.4:c.7454-54_7454-53insAGGGAAG , LRG_778t1:c.7454-54_7454-53insAGGGAAG NP_000129.3:n.7454-54_7454-53insAGGGAAG
NM_000138.5:c.7454-54_7454-53insAGGGAAG MANE Select NP_000129.3:n.7454-54_7454-53insAGGGAAG