Canonical Allele Identifier: CA392323422

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48415747C>G , CM000677.2:g.48415747C>G	GRCh38
NC_000015.9:g.48707944C>G , CM000677.1:g.48707944C>G	GRCh37
NC_000015.8:g.46495236C>G	NCBI36
NG_008805.2:g.235042G>C , LRG_778:g.235042G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000138.5:c.7840G>C MANE Select	NP_000129.3:p.Ala2614Pro
ENST00000316623.10:c.7840G>C MANE Select	ENSP00000325527.5:p.Ala2614Pro
NM_000138.4:c.7840G>C , LRG_778t1:c.7840G>C	NP_000129.3:p.Ala2614Pro
ENST00000316623.9:c.7840G>C	ENSP00000325527.5:p.Ala2614Pro
ENST00000559133.5:c.3209G>C
ENST00000559133.6:c.*648G>C	ENSP00000453958.2:n.*648G>C
ENST00000561429.1:n.95G>C
ENST00000674301.1:c.3006G>C	ENSP00000501333.1:n.3006G>C
ENST00000674301.2:c.*1353G>C	ENSP00000501333.2:n.*1353G>C
ENST00000682158.1:n.1221G>C
ENST00000682170.1:n.2021G>C
ENST00000682767.1:n.1137G>C