Canonical Allele Identifier: CA392317769

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48764804T>G (hg19) ; chr15:g.48472607T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48472607T>G , CM000677.2:g.48472607T>G	GRCh38
NC_000015.9:g.48764804T>G , CM000677.1:g.48764804T>G	GRCh37
NC_000015.8:g.46552096T>G	NCBI36
NG_008805.2:g.178182A>C , LRG_778:g.178182A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.4280A>C	ENSP00000453958.2:p.Tyr1427Ser
ENST00000674301.2:c.4280A>C	ENSP00000501333.2:p.Tyr1427Ser
ENST00000683268.1:n.247A>C
ENST00000684448.1:n.2954A>C
ENST00000316623.10:c.4280A>C MANE Select	ENSP00000325527.5:p.Tyr1427Ser
ENST00000316623.9:c.4280A>C	ENSP00000325527.5:p.Tyr1427Ser
ENST00000537463.6:c.*43A>C	ENSP00000440294.2:n.*43A>C
NM_000138.4:c.4280A>C , LRG_778t1:c.4280A>C	NP_000129.3:p.Tyr1427Ser
NM_000138.5:c.4280A>C MANE Select	NP_000129.3:p.Tyr1427Ser