Canonical Allele Identifier: CA392347856
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48520784G>T , CM000677.2:g.48520784G>T GRCh38
NC_000015.9:g.48812981G>T , CM000677.1:g.48812981G>T GRCh37
NC_000015.8:g.46600273G>T NCBI36
NG_008805.2:g.130005C>A , LRG_778:g.130005C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.1022C>A ENSP00000453958.2:p.Thr341Lys
ENST00000674301.2:c.1022C>A ENSP00000501333.2:p.Thr341Lys
ENST00000316623.10:c.1022C>A MANE Select ENSP00000325527.5:p.Thr341Lys
ENST00000316623.9:c.1022C>A ENSP00000325527.5:p.Thr341Lys
ENST00000537463.6:c.636+16927C>A ENSP00000440294.2:n.636+16927C>A
NM_000138.4:c.1022C>A , LRG_778t1:c.1022C>A NP_000129.3:p.Thr341Lys
NM_000138.5:c.1022C>A MANE Select NP_000129.3:p.Thr341Lys