Canonical Allele Identifier: CA392328103
Community Standard Title: NM_000138.5(FBN1):c.7331-1G>A
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48425492C>T , CM000677.2:g.48425492C>T GRCh38
NC_000015.9:g.48717689C>T , CM000677.1:g.48717689C>T GRCh37
NC_000015.8:g.46504981C>T NCBI36
NG_008805.2:g.225297G>A , LRG_778:g.225297G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.7331-1G>A MANE Select NP_000129.3:n.7331-1G>A
ENST00000316623.10:c.7331-1G>A MANE Select ENSP00000325527.5:n.7331-1G>A
NM_000138.4:c.7331-1G>A , LRG_778t1:c.7331-1G>A NP_000129.3:n.7331-1G>A
ENST00000316623.9:c.7331-1G>A ENSP00000325527.5:n.7331-1G>A
ENST00000559133.5:c.2700-1G>A
ENST00000559133.6:c.*139-1G>A ENSP00000453958.2:n.*139-1G>A
ENST00000674301.1:c.2497-1G>A ENSP00000501333.1:n.2497-1G>A
ENST00000674301.2:c.*844-1G>A ENSP00000501333.2:n.*844-1G>A
ENST00000682170.1:n.1512-1G>A
ENST00000682767.1:n.628-1G>A