Canonical Allele Identifier: CA392322523

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48707748A>C (hg19) ; chr15:g.48415551A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48415551A>C , CM000677.2:g.48415551A>C	GRCh38
NC_000015.9:g.48707748A>C , CM000677.1:g.48707748A>C	GRCh37
NC_000015.8:g.46495040A>C	NCBI36
NG_008805.2:g.235238T>G , LRG_778:g.235238T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*844T>G	ENSP00000453958.2:n.*844T>G
ENST00000674301.2:c.*1549T>G	ENSP00000501333.2:n.*1549T>G
ENST00000682158.1:n.1417T>G
ENST00000682170.1:n.2217T>G
ENST00000682767.1:n.1333T>G
ENST00000316623.10:c.8036T>G MANE Select	ENSP00000325527.5:p.Phe2679Cys
ENST00000674301.1:c.3202T>G	ENSP00000501333.1:n.3202T>G
ENST00000316623.9:c.8036T>G	ENSP00000325527.5:p.Phe2679Cys
ENST00000559133.5:c.3405T>G
ENST00000561429.1:n.291T>G
NM_000138.4:c.8036T>G , LRG_778t1:c.8036T>G	NP_000129.3:p.Phe2679Cys
NM_000138.5:c.8036T>G MANE Select	NP_000129.3:p.Phe2679Cys