Canonical Allele Identifier: CA392337278
Community Standard Title: NM_000138.5(FBN1):c.6180C>G (p.Tyr2060Ter)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48437901G>C , CM000677.2:g.48437901G>C GRCh38
NC_000015.9:g.48730098G>C , CM000677.1:g.48730098G>C GRCh37
NC_000015.8:g.46517390G>C NCBI36
NG_008805.2:g.212888C>G , LRG_778:g.212888C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.6180C>G MANE Select NP_000129.3:p.Tyr2060Ter
ENST00000316623.10:c.6180C>G MANE Select ENSP00000325527.5:p.Tyr2060Ter
NM_000138.4:c.6180C>G , LRG_778t1:c.6180C>G NP_000129.3:p.Tyr2060Ter
ENST00000316623.9:c.6180C>G ENSP00000325527.5:p.Tyr2060Ter
ENST00000537463.6:c.*1943C>G ENSP00000440294.2:n.*1943C>G
ENST00000559133.5:c.1487C>G
ENST00000559133.6:c.6180C>G ENSP00000453958.2:p.Tyr2060Ter
ENST00000560820.1:n.300C>G
ENST00000674301.1:c.1179C>G ENSP00000501333.1:p.Tyr393Ter
ENST00000674301.2:c.6180C>G ENSP00000501333.2:p.Tyr2060Ter