Canonical Allele Identifier: CA392325911

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48714188A>T (hg19) ; chr15:g.48421991A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48421991A>T , CM000677.2:g.48421991A>T	GRCh38
NC_000015.9:g.48714188A>T , CM000677.1:g.48714188A>T	GRCh37
NC_000015.8:g.46501480A>T	NCBI36
NG_008805.2:g.228798T>A , LRG_778:g.228798T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*339T>A	ENSP00000453958.2:n.*339T>A
ENST00000674301.2:c.*1044T>A	ENSP00000501333.2:n.*1044T>A
ENST00000682170.1:n.1712T>A
ENST00000682767.1:n.828T>A
ENST00000316623.10:c.7531T>A MANE Select	ENSP00000325527.5:p.Cys2511Ser
ENST00000674301.1:c.2697T>A	ENSP00000501333.1:n.2697T>A
ENST00000316623.9:c.7531T>A	ENSP00000325527.5:p.Cys2511Ser
ENST00000559133.5:c.2900T>A
NM_000138.4:c.7531T>A , LRG_778t1:c.7531T>A	NP_000129.3:p.Cys2511Ser
NM_000138.5:c.7531T>A MANE Select	NP_000129.3:p.Cys2511Ser