Canonical Allele Identifier: CA392349123

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48463124C>G , CM000677.2:g.48463124C>G	GRCh38
NC_000015.9:g.48755321C>G , CM000677.1:g.48755321C>G	GRCh37
NC_000015.8:g.46542613C>G	NCBI36
NG_008805.2:g.187665G>C , LRG_778:g.187665G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000138.5:c.5182G>C MANE Select	NP_000129.3:p.Ala1728Pro
ENST00000316623.10:c.5182G>C MANE Select	ENSP00000325527.5:p.Ala1728Pro
NM_000138.4:c.5182G>C , LRG_778t1:c.5182G>C	NP_000129.3:p.Ala1728Pro
ENST00000316623.9:c.5182G>C	ENSP00000325527.5:p.Ala1728Pro
ENST00000537463.6:c.*945G>C	ENSP00000440294.2:n.*945G>C
ENST00000559133.5:c.489G>C
ENST00000559133.6:c.5182G>C	ENSP00000453958.2:p.Ala1728Pro
ENST00000674301.1:c.181G>C	ENSP00000501333.1:p.Ala61Pro
ENST00000674301.2:c.5182G>C	ENSP00000501333.2:p.Ala1728Pro
ENST00000684448.1:n.3856G>C