Canonical Allele Identifier: CA392330102
Community Standard Title: NM_000138.5(FBN1):c.7064G>C (p.Arg2355Thr)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48427707C>G , CM000677.2:g.48427707C>G GRCh38
NC_000015.9:g.48719904C>G , CM000677.1:g.48719904C>G GRCh37
NC_000015.8:g.46507196C>G NCBI36
NG_008805.2:g.223082G>C , LRG_778:g.223082G>C

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.7064G>C MANE Select NP_000129.3:p.Arg2355Thr
ENST00000316623.10:c.7064G>C MANE Select ENSP00000325527.5:p.Arg2355Thr
NM_000138.4:c.7064G>C , LRG_778t1:c.7064G>C NP_000129.3:p.Arg2355Thr
ENST00000316623.9:c.7064G>C ENSP00000325527.5:p.Arg2355Thr
ENST00000559133.5:c.2433G>C
ENST00000559133.6:c.7126G>C ENSP00000453958.2:p.Gly2376Arg
ENST00000674301.1:c.2230G>C ENSP00000501333.1:n.2230G>C
ENST00000674301.2:c.*577G>C ENSP00000501333.2:n.*577G>C
ENST00000682170.1:n.1245G>C
ENST00000682767.1:n.361G>C