Canonical Allele Identifier: CA392329922

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48427683C>G , CM000677.2:g.48427683C>G	GRCh38
NC_000015.9:g.48719880C>G , CM000677.1:g.48719880C>G	GRCh37
NC_000015.8:g.46507172C>G	NCBI36
NG_008805.2:g.223106G>C , LRG_778:g.223106G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000138.5:c.7088G>C MANE Select	NP_000129.3:p.Cys2363Ser
ENST00000316623.10:c.7088G>C MANE Select	ENSP00000325527.5:p.Cys2363Ser
NM_000138.4:c.7088G>C , LRG_778t1:c.7088G>C	NP_000129.3:p.Cys2363Ser
ENST00000316623.9:c.7088G>C	ENSP00000325527.5:p.Cys2363Ser
ENST00000559133.5:c.2457G>C
ENST00000559133.6:c.7150G>C	ENSP00000453958.2:p.Ala2384Pro
ENST00000674301.1:c.2254G>C	ENSP00000501333.1:n.2254G>C
ENST00000674301.2:c.*601G>C	ENSP00000501333.2:n.*601G>C
ENST00000682170.1:n.1269G>C
ENST00000682767.1:n.385G>C