Canonical Allele Identifier: CA392335004
Community Standard Title: NM_000138.5(FBN1):c.6549T>A (p.Asn2183Lys)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48434661A>T , CM000677.2:g.48434661A>T GRCh38
NC_000015.9:g.48726858A>T , CM000677.1:g.48726858A>T GRCh37
NC_000015.8:g.46514150A>T NCBI36
NG_008805.2:g.216128T>A , LRG_778:g.216128T>A

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.6549T>A MANE Select NP_000129.3:p.Asn2183Lys
ENST00000316623.10:c.6549T>A MANE Select ENSP00000325527.5:p.Asn2183Lys
NM_000138.4:c.6549T>A , LRG_778t1:c.6549T>A NP_000129.3:p.Asn2183Lys
ENST00000316623.9:c.6549T>A ENSP00000325527.5:p.Asn2183Lys
ENST00000537463.6:c.*2312T>A ENSP00000440294.2:n.*2312T>A
ENST00000559133.5:c.1856T>A
ENST00000559133.6:c.6549T>A ENSP00000453958.2:p.Asn2183Lys
ENST00000674301.1:c.1548T>A ENSP00000501333.1:p.Asn516Lys
ENST00000674301.2:c.6549T>A ENSP00000501333.2:p.Asn2183Lys
ENST00000682170.1:n.158T>A