Canonical Allele Identifier: CA392330571

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48720581T>G (hg19) ; chr15:g.48428384T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48428384T>G , CM000677.2:g.48428384T>G	GRCh38
NC_000015.9:g.48720581T>G , CM000677.1:g.48720581T>G	GRCh37
NC_000015.8:g.46507873T>G	NCBI36
NG_008805.2:g.222405A>C , LRG_778:g.222405A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6959A>C	ENSP00000453958.2:p.Asp2320Ala
ENST00000674301.2:c.*410A>C	ENSP00000501333.2:n.*410A>C
ENST00000682170.1:n.568A>C
ENST00000682767.1:n.194A>C
ENST00000316623.10:c.6959A>C MANE Select	ENSP00000325527.5:p.Asp2320Ala
ENST00000674301.1:c.2063A>C	ENSP00000501333.1:n.2063A>C
ENST00000316623.9:c.6959A>C	ENSP00000325527.5:p.Asp2320Ala
ENST00000559133.5:c.2266A>C
ENST00000560720.1:n.246A>C
NM_000138.4:c.6959A>C , LRG_778t1:c.6959A>C	NP_000129.3:p.Asp2320Ala
NM_000138.5:c.6959A>C MANE Select	NP_000129.3:p.Asp2320Ala