Canonical Allele Identifier: CA015998

Gene: FBN1

Linked Data

• ClinVar Variation Id: 42390
• ClinVar RCV Id: RCV000035232
• dbSNP Id: rs397515826
• MyVariant Identifiers: chr15:g.48738970G>C (hg19) ; chr15:g.48446773G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48446773G>C , CM000677.2:g.48446773G>C	GRCh38
NC_000015.9:g.48738970G>C , CM000677.1:g.48738970G>C	GRCh37
NC_000015.8:g.46526262G>C	NCBI36
NG_008805.2:g.204016C>G , LRG_778:g.204016C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.5721C>G	ENSP00000453958.2:p.Asn1907Lys
ENST00000674301.2:c.5721C>G	ENSP00000501333.2:p.Asn1907Lys
ENST00000684448.1:n.4395C>G
ENST00000316623.10:c.5721C>G MANE Select	ENSP00000325527.5:p.Asn1907Lys
ENST00000674301.1:c.720C>G	ENSP00000501333.1:p.Asn240Lys
ENST00000316623.9:c.5721C>G	ENSP00000325527.5:p.Asn1907Lys
ENST00000537463.6:c.*1484C>G	ENSP00000440294.2:n.*1484C>G
ENST00000559133.5:c.1028C>G
NM_000138.4:c.5721C>G , LRG_778t1:c.5721C>G	NP_000129.3:p.Asn1907Lys
NM_000138.5:c.5721C>G MANE Select	NP_000129.3:p.Asn1907Lys