Canonical Allele Identifier: CA392346544
Community Standard Title: NM_000138.5(FBN1):c.5304T>G (p.Asp1768Glu)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48456755A>C , CM000677.2:g.48456755A>C GRCh38
NC_000015.9:g.48748952A>C , CM000677.1:g.48748952A>C GRCh37
NC_000015.8:g.46536244A>C NCBI36
NG_008805.2:g.194034T>G , LRG_778:g.194034T>G

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.5304T>G MANE Select NP_000129.3:p.Asp1768Glu
ENST00000316623.10:c.5304T>G MANE Select ENSP00000325527.5:p.Asp1768Glu
NM_000138.4:c.5304T>G , LRG_778t1:c.5304T>G NP_000129.3:p.Asp1768Glu
ENST00000316623.9:c.5304T>G ENSP00000325527.5:p.Asp1768Glu
ENST00000537463.6:c.*1067T>G ENSP00000440294.2:n.*1067T>G
ENST00000559133.5:c.611T>G
ENST00000559133.6:c.5304T>G ENSP00000453958.2:p.Asp1768Glu
ENST00000674301.1:c.303T>G ENSP00000501333.1:p.Asp101Glu
ENST00000674301.2:c.5304T>G ENSP00000501333.2:p.Asp1768Glu
ENST00000684448.1:n.3978T>G