Canonical Allele Identifier: CA2175529416
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs2043737043

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48509032_48509033del , CM000677.2:g.48509032_48509033del GRCh38
NC_000015.9:g.48801229_48801230del , CM000677.1:g.48801229_48801230del GRCh37
NC_000015.8:g.46588521_46588522del NCBI36
NG_008805.2:g.141756_141757del , LRG_778:g.141756_141757del

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.1715-329_1715-328del ENSP00000453958.2:n.1715-329_1715-328del
ENST00000674301.2:c.1715-329_1715-328del ENSP00000501333.2:n.1715-329_1715-328del
ENST00000684448.1:n.389-329_389-328del
ENST00000316623.10:c.1715-329_1715-328del MANE Select ENSP00000325527.5:n.1715-329_1715-328del
ENST00000316623.9:c.1715-329_1715-328del ENSP00000325527.5:n.1715-329_1715-328del
ENST00000537463.6:c.636+28678_636+28679del ENSP00000440294.2:n.636+28678_636+28679del
NM_000138.4:c.1715-329_1715-328del , LRG_778t1:c.1715-329_1715-328del NP_000129.3:n.1715-329_1715-328del
NM_000138.5:c.1715-329_1715-328del MANE Select NP_000129.3:n.1715-329_1715-328del