Canonical Allele Identifier: CA915946637

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48429432T>C , CM000677.2:g.48429432T>C	GRCh38
NC_000015.9:g.48721629T>C , CM000677.1:g.48721629T>C	GRCh37
NC_000015.8:g.46508921T>C	NCBI36
NG_008805.2:g.221357A>G , LRG_778:g.221357A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000138.5:c.6872-961A>G MANE Select	NP_000129.3:n.6872-961A>G
ENST00000316623.10:c.6872-961A>G MANE Select	ENSP00000325527.5:n.6872-961A>G
NM_000138.4:c.6872-961A>G , LRG_778t1:c.6872-961A>G	NP_000129.3:n.6872-961A>G
ENST00000316623.9:c.6872-961A>G	ENSP00000325527.5:n.6872-961A>G
ENST00000559133.5:c.2179-961A>G
ENST00000559133.6:c.6872-961A>G	ENSP00000453958.2:n.6872-961A>G
ENST00000560720.1:n.159-961A>G
ENST00000674301.1:c.1976-961A>G	ENSP00000501333.1:n.1976-961A>G
ENST00000674301.2:c.*323-961A>G	ENSP00000501333.2:n.*323-961A>G
ENST00000682170.1:n.481-961A>G