Canonical Allele Identifier: CA2175511746
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48485393A= , CM000677.2:g.48485393A= GRCh38
NC_000015.9:g.48777590A= , CM000677.1:g.48777590A= GRCh37
NC_000015.8:g.46564882A= NCBI36
NG_008805.2:g.165396T= , LRG_778:g.165396T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.3693T= ENSP00000453958.2:p.Pro1231=
ENST00000674301.2:c.3693T= ENSP00000501333.2:p.Pro1231=
ENST00000684448.1:n.2367T=
ENST00000316623.10:c.3693T= MANE Select ENSP00000325527.5:p.Pro1231=
ENST00000316623.9:c.3693T= ENSP00000325527.5:p.Pro1231=
ENST00000537463.6:c.637-10743T= ENSP00000440294.2:n.637-10743T=
NM_000138.4:c.3693T= , LRG_778t1:c.3693T= NP_000129.3:p.Pro1231=
NM_000138.5:c.3693T= MANE Select NP_000129.3:p.Pro1231=