Canonical Allele Identifier: CA392338459

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48734008C>G (hg19) ; chr15:g.48441811C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48441811C>G , CM000677.2:g.48441811C>G	GRCh38
NC_000015.9:g.48734008C>G , CM000677.1:g.48734008C>G	GRCh37
NC_000015.8:g.46521300C>G	NCBI36
NG_008805.2:g.208978G>C , LRG_778:g.208978G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6073G>C	ENSP00000453958.2:p.Ala2025Pro
ENST00000674301.2:c.6073G>C	ENSP00000501333.2:p.Ala2025Pro
ENST00000316623.10:c.6073G>C MANE Select	ENSP00000325527.5:p.Ala2025Pro
ENST00000674301.1:c.1072G>C	ENSP00000501333.1:p.Ala358Pro
ENST00000316623.9:c.6073G>C	ENSP00000325527.5:p.Ala2025Pro
ENST00000537463.6:c.*1836G>C	ENSP00000440294.2:n.*1836G>C
ENST00000559133.5:c.1380G>C
ENST00000560820.1:n.193G>C
NM_000138.4:c.6073G>C , LRG_778t1:c.6073G>C	NP_000129.3:p.Ala2025Pro
NM_000138.5:c.6073G>C MANE Select	NP_000129.3:p.Ala2025Pro