Canonical Allele Identifier: CA269526064

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48436951T>G , CM000677.2:g.48436951T>G	GRCh38
NC_000015.9:g.48729148T>G , CM000677.1:g.48729148T>G	GRCh37
NC_000015.8:g.46516440T>G	NCBI36
NG_008805.2:g.213838A>C , LRG_778:g.213838A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6496+10A>C	ENSP00000453958.2:n.6496+10A>C
ENST00000674301.2:c.6496+10A>C	ENSP00000501333.2:n.6496+10A>C
ENST00000682170.1:n.105+10A>C
ENST00000316623.10:c.6496+10A>C MANE Select	ENSP00000325527.5:n.6496+10A>C
ENST00000674301.1:c.1495+10A>C	ENSP00000501333.1:n.1495+10A>C
ENST00000316623.9:c.6496+10A>C	ENSP00000325527.5:n.6496+10A>C
ENST00000537463.6:c.*2259+10A>C	ENSP00000440294.2:n.*2259+10A>C
ENST00000559133.5:c.1803+10A>C
NM_000138.4:c.6496+10A>C , LRG_778t1:c.6496+10A>C	NP_000129.3:n.6496+10A>C
NM_000138.5:c.6496+10A>C MANE Select	NP_000129.3:n.6496+10A>C