Canonical Allele Identifier: CA392340045

Gene: FBN1

Linked Data

• gnomAD v4: 15-48445432-A-G
• MyVariant Identifiers: chr15:g.48737629A>G (hg19) ; chr15:g.48445432A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48445432A>G , CM000677.2:g.48445432A>G	GRCh38
NC_000015.9:g.48737629A>G , CM000677.1:g.48737629A>G	GRCh37
NC_000015.8:g.46524921A>G	NCBI36
NG_008805.2:g.205357T>C , LRG_778:g.205357T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.5861T>C	ENSP00000453958.2:p.Phe1954Ser
ENST00000674301.2:c.5861T>C	ENSP00000501333.2:p.Phe1954Ser
ENST00000684448.1:n.4535T>C
ENST00000316623.10:c.5861T>C MANE Select	ENSP00000325527.5:p.Phe1954Ser
ENST00000674301.1:c.860T>C	ENSP00000501333.1:p.Phe287Ser
ENST00000316623.9:c.5861T>C	ENSP00000325527.5:p.Phe1954Ser
ENST00000537463.6:c.*1624T>C	ENSP00000440294.2:n.*1624T>C
ENST00000559133.5:c.1168T>C
NM_000138.4:c.5861T>C , LRG_778t1:c.5861T>C	NP_000129.3:p.Phe1954Ser
NM_000138.5:c.5861T>C MANE Select	NP_000129.3:p.Phe1954Ser