Canonical Allele Identifier: CA2175498694
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48428558T= , CM000677.2:g.48428558T= GRCh38
NC_000015.9:g.48720755T= , CM000677.1:g.48720755T= GRCh37
NC_000015.8:g.46508047T= NCBI36
NG_008805.2:g.222231A= , LRG_778:g.222231A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.6872-87A= ENSP00000453958.2:n.6872-87A=
ENST00000674301.2:c.*323-87A= ENSP00000501333.2:n.*323-87A=
ENST00000682170.1:n.481-87A=
ENST00000682767.1:n.20A=
ENST00000316623.10:c.6872-87A= MANE Select ENSP00000325527.5:n.6872-87A=
ENST00000674301.1:c.1976-87A= ENSP00000501333.1:n.1976-87A=
ENST00000316623.9:c.6872-87A= ENSP00000325527.5:n.6872-87A=
ENST00000559133.5:c.2179-87A=
ENST00000560720.1:n.159-87A=
NM_000138.4:c.6872-87A= , LRG_778t1:c.6872-87A= NP_000129.3:n.6872-87A=
NM_000138.5:c.6872-87A= MANE Select NP_000129.3:n.6872-87A=