Canonical Allele Identifier: CA9150661

Gene: FBN3 ELAVL1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8072150C>T , CM000681.2:g.8072150C>T	GRCh38
NC_000019.9:g.8137034C>T , CM000681.1:g.8137034C>T	GRCh37
NC_000019.8:g.8043034C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000600128.6:c.7986G>A (FBN3) MANE Select	ENSP00000470498.1:p.Pro2662=
ENST00000651877.1:c.8112G>A (FBN3)	ENSP00000498507.1:p.Pro2704=
ENST00000270509.6:c.7986G>A (FBN3)	ENSP00000270509.2:p.Pro2662=
ENST00000351593.9:c.-20+77154G>A (ELAVL1)	ENSP00000264073.6:n.-20+77154G>A
ENST00000600128.5:c.7986G>A (FBN3)	ENSP00000470498.1:p.Pro2662=
ENST00000601739.5:c.7986G>A (FBN3)	ENSP00000472324.1:p.Pro2662=
NM_032447.3:c.7986G>A (FBN3)	NP_115823.3:p.Pro2662=
XM_011528373.1:c.7986G>A (FBN3)	XP_011526675.1:p.Pro2662=
NM_001321431.1:c.7986G>A (FBN3)	NP_001308360.1:p.Pro2662=
NM_032447.4:c.7986G>A (FBN3)	NP_115823.3:p.Pro2662=
XM_017027372.1:c.7986G>A (FBN3)	XP_016882861.1:p.Pro2662=
XM_017027373.1:c.7926G>A (FBN3)	XP_016882862.1:p.Pro2642=
XM_017027374.2:c.7890G>A (FBN3)	XP_016882863.1:p.Pro2630=
XM_017027375.2:c.7863G>A (FBN3)	XP_016882864.1:p.Pro2621=
XM_017027376.1:c.7857G>A (FBN3)	XP_016882865.1:p.Pro2619=
XM_017027377.2:c.5403G>A (FBN3)	XP_016882866.1:p.Pro1801=
XM_017027378.2:c.4344G>A (FBN3)	XP_016882867.1:p.Pro1448=
XM_017027379.1:c.8112G>A (FBN3)	XP_016882868.1:p.Pro2704=
NM_032447.5:c.7986G>A (FBN3) MANE Select	NP_115823.3:p.Pro2662=
NM_001321431.2:c.7986G>A (FBN3)	NP_001308360.1:p.Pro2662=