Canonical Allele Identifier: CA9150569
Community Standard Title: NM_032447.5(FBN3):c.8304G>T (p.Pro2768=)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8066045C>A , CM000681.2:g.8066045C>A GRCh38
NC_000019.9:g.8130929C>A , CM000681.1:g.8130929C>A GRCh37
NC_000019.8:g.8036929C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_032447.5:c.8304G>T (FBN3) MANE Select NP_115823.3:p.Pro2768=
ENST00000600128.6:c.8304G>T (FBN3) MANE Select ENSP00000470498.1:p.Pro2768=
NM_001321431.1:c.8304G>T (FBN3) NP_001308360.1:p.Pro2768=
NM_001321431.2:c.8304G>T (FBN3) NP_001308360.1:p.Pro2768=
NM_032447.3:c.8304G>T (FBN3) NP_115823.3:p.Pro2768=
NM_032447.4:c.8304G>T (FBN3) NP_115823.3:p.Pro2768=
ENST00000270509.6:c.8304G>T (FBN3) ENSP00000270509.2:p.Pro2768=
ENST00000351593.9:c.-19-74211G>T (ELAVL1) ENSP00000264073.6:n.-19-74211G>T
ENST00000600128.5:c.8304G>T (FBN3) ENSP00000470498.1:p.Pro2768=
ENST00000601739.5:c.8304G>T (FBN3) ENSP00000472324.1:p.Pro2768=
ENST00000651877.1:c.8430G>T (FBN3) ENSP00000498507.1:p.Pro2810=
XM_011528373.1:c.8304G>T (FBN3) XP_011526675.1:p.Pro2768=
XM_017027372.1:c.8304G>T (FBN3) XP_016882861.1:p.Pro2768=
XM_017027373.1:c.8244G>T (FBN3) XP_016882862.1:p.Pro2748=
XM_017027374.2:c.8208G>T (FBN3) XP_016882863.1:p.Pro2736=
XM_017027375.2:c.8181G>T (FBN3) XP_016882864.1:p.Pro2727=
XM_017027376.1:c.8175G>T (FBN3) XP_016882865.1:p.Pro2725=
XM_017027377.2:c.5721G>T (FBN3) XP_016882866.1:p.Pro1907=
XM_017027378.2:c.4662G>T (FBN3) XP_016882867.1:p.Pro1554=
XM_017027379.1:c.8430G>T (FBN3) XP_016882868.1:p.Pro2810=