Canonical Allele Identifier: CA2628334224

Gene: FBN1

Linked Data

• gnomAD v4: 15-48441586-CATT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48441588_48441590del , CM000677.2:g.48441588_48441590del	GRCh38
NC_000015.9:g.48733785_48733787del , CM000677.1:g.48733785_48733787del	GRCh37
NC_000015.8:g.46521077_46521079del	NCBI36
NG_008805.2:g.209200_209202del , LRG_778:g.209200_209202del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6163+132_6163+134del	ENSP00000453958.2:n.6163+132_6163+134del
ENST00000674301.2:c.6163+132_6163+134del	ENSP00000501333.2:n.6163+132_6163+134del
ENST00000316623.10:c.6163+132_6163+134del MANE Select	ENSP00000325527.5:n.6163+132_6163+134del
ENST00000674301.1:c.1162+132_1162+134del	ENSP00000501333.1:n.1162+132_1162+134del
ENST00000316623.9:c.6163+132_6163+134del	ENSP00000325527.5:n.6163+132_6163+134del
ENST00000537463.6:c.*1926+132_*1926+134del	ENSP00000440294.2:n.*1926+132_*1926+134del
ENST00000559133.5:c.1470+132_1470+134del
ENST00000560820.1:n.283+132_283+134del
NM_000138.4:c.6163+132_6163+134del , LRG_778t1:c.6163+132_6163+134del	NP_000129.3:n.6163+132_6163+134del
NM_000138.5:c.6163+132_6163+134del MANE Select	NP_000129.3:n.6163+132_6163+134del