Canonical Allele Identifier: CA505255786

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8072081G>A , CM000681.2:g.8072081G>A GRCh38
NC_000019.9:g.8136965G>A , CM000681.1:g.8136965G>A GRCh37
NC_000019.8:g.8042965G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000600128.6:c.8055C>T (FBN3) MANE Select ENSP00000470498.1:p.Asp2685=
ENST00000651877.1:c.8181C>T (FBN3) ENSP00000498507.1:p.Asp2727=
ENST00000270509.6:c.8055C>T (FBN3) ENSP00000270509.2:p.Asp2685=
ENST00000351593.9:c.-20+77223C>T (ELAVL1) ENSP00000264073.6:n.-20+77223C>T
ENST00000600128.5:c.8055C>T (FBN3) ENSP00000470498.1:p.Asp2685=
ENST00000601739.5:c.8055C>T (FBN3) ENSP00000472324.1:p.Asp2685=
NM_032447.3:c.8055C>T (FBN3) NP_115823.3:p.Asp2685=
XM_011528373.1:c.8055C>T (FBN3) XP_011526675.1:p.Asp2685=
NM_001321431.1:c.8055C>T (FBN3) NP_001308360.1:p.Asp2685=
NM_032447.4:c.8055C>T (FBN3) NP_115823.3:p.Asp2685=
XM_017027372.1:c.8055C>T (FBN3) XP_016882861.1:p.Asp2685=
XM_017027373.1:c.7995C>T (FBN3) XP_016882862.1:p.Asp2665=
XM_017027374.2:c.7959C>T (FBN3) XP_016882863.1:p.Asp2653=
XM_017027375.2:c.7932C>T (FBN3) XP_016882864.1:p.Asp2644=
XM_017027376.1:c.7926C>T (FBN3) XP_016882865.1:p.Asp2642=
XM_017027377.2:c.5472C>T (FBN3) XP_016882866.1:p.Asp1824=
XM_017027378.2:c.4413C>T (FBN3) XP_016882867.1:p.Asp1471=
XM_017027379.1:c.8181C>T (FBN3) XP_016882868.1:p.Asp2727=
NM_032447.5:c.8055C>T (FBN3) MANE Select NP_115823.3:p.Asp2685=
NM_001321431.2:c.8055C>T (FBN3) NP_001308360.1:p.Asp2685=