Canonical Allele Identifier: CA392340259

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48737696C>T (hg19) ; chr15:g.48445499C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48445499C>T , CM000677.2:g.48445499C>T	GRCh38
NC_000015.9:g.48737696C>T , CM000677.1:g.48737696C>T	GRCh37
NC_000015.8:g.46524988C>T	NCBI36
NG_008805.2:g.205290G>A , LRG_778:g.205290G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.5794G>A	ENSP00000453958.2:p.Asp1932Asn
ENST00000674301.2:c.5794G>A	ENSP00000501333.2:p.Asp1932Asn
ENST00000684448.1:n.4468G>A
ENST00000316623.10:c.5794G>A MANE Select	ENSP00000325527.5:p.Asp1932Asn
ENST00000674301.1:c.793G>A	ENSP00000501333.1:p.Asp265Asn
ENST00000316623.9:c.5794G>A	ENSP00000325527.5:p.Asp1932Asn
ENST00000537463.6:c.*1557G>A	ENSP00000440294.2:n.*1557G>A
ENST00000559133.5:c.1101G>A
NM_000138.4:c.5794G>A , LRG_778t1:c.5794G>A	NP_000129.3:p.Asp1932Asn
NM_000138.5:c.5794G>A MANE Select	NP_000129.3:p.Asp1932Asn