Canonical Allele Identifier: CA2628329839
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48487028_48487034del , CM000677.2:g.48487028_48487034del GRCh38
NC_000015.9:g.48779225_48779231del , CM000677.1:g.48779225_48779231del GRCh37
NC_000015.8:g.46566517_46566523del NCBI36
NG_008805.2:g.163755_163761del , LRG_778:g.163755_163761del

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.3589+41_3589+47del ENSP00000453958.2:n.3589+41_3589+47del
ENST00000674301.2:c.3589+41_3589+47del ENSP00000501333.2:n.3589+41_3589+47del
ENST00000684448.1:n.2263+41_2263+47del
ENST00000316623.10:c.3589+41_3589+47del MANE Select ENSP00000325527.5:n.3589+41_3589+47del
ENST00000316623.9:c.3589+41_3589+47del ENSP00000325527.5:n.3589+41_3589+47del
ENST00000537463.6:c.637-12384_637-12378del ENSP00000440294.2:n.637-12384_637-12378del
NM_000138.4:c.3589+41_3589+47del , LRG_778t1:c.3589+41_3589+47del NP_000129.3:n.3589+41_3589+47del
NM_000138.5:c.3589+41_3589+47del MANE Select NP_000129.3:n.3589+41_3589+47del