Canonical Allele Identifier: CA059637
Community Standard Title: NM_000138.5(FBN1):c.8123A>G (p.Asn2708Ser)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48412672T>C , CM000677.2:g.48412672T>C GRCh38
NC_000015.9:g.48704869T>C , CM000677.1:g.48704869T>C GRCh37
NC_000015.8:g.46492161T>C NCBI36
NG_008805.2:g.238117A>G , LRG_778:g.238117A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.8123A>G MANE Select NP_000129.3:p.Asn2708Ser
ENST00000316623.10:c.8123A>G MANE Select ENSP00000325527.5:p.Asn2708Ser
NM_000138.4:c.8123A>G , LRG_778t1:c.8123A>G NP_000129.3:p.Asn2708Ser
ENST00000316623.9:c.8123A>G ENSP00000325527.5:p.Asn2708Ser
ENST00000559133.5:c.3492A>G
ENST00000559133.6:c.*931A>G ENSP00000453958.2:n.*931A>G
ENST00000561429.1:n.378A>G
ENST00000674301.1:c.3289A>G ENSP00000501333.1:n.3289A>G
ENST00000674301.2:c.*1636A>G ENSP00000501333.2:n.*1636A>G
ENST00000682158.1:n.1504A>G
ENST00000682170.1:n.2304A>G
ENST00000682767.1:n.1420A>G