Canonical Allele Identifier: CA2175511740

Gene: FBN1

Linked Data

• dbSNP Id: rs2043137887

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48444376_48444377del , CM000677.2:g.48444376_48444377del	GRCh38
NC_000015.9:g.48736573_48736574del , CM000677.1:g.48736573_48736574del	GRCh37
NC_000015.8:g.46523865_46523866del	NCBI36
NG_008805.2:g.206413_206414del , LRG_778:g.206413_206414del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6037+165_6037+166del	ENSP00000453958.2:n.6037+165_6037+166del
ENST00000674301.2:c.6037+165_6037+166del	ENSP00000501333.2:n.6037+165_6037+166del
ENST00000684448.1:n.4876_4877del
ENST00000316623.10:c.6037+165_6037+166del MANE Select	ENSP00000325527.5:n.6037+165_6037+166del
ENST00000674301.1:c.1036+165_1036+166del	ENSP00000501333.1:n.1036+165_1036+166del
ENST00000316623.9:c.6037+165_6037+166del	ENSP00000325527.5:n.6037+165_6037+166del
ENST00000537463.6:c.*1800+165_*1800+166del	ENSP00000440294.2:n.*1800+165_*1800+166del
ENST00000559133.5:c.1344+165_1344+166del
ENST00000560820.1:n.157+165_157+166del
NM_000138.4:c.6037+165_6037+166del , LRG_778t1:c.6037+165_6037+166del	NP_000129.3:n.6037+165_6037+166del
NM_000138.5:c.6037+165_6037+166del MANE Select	NP_000129.3:n.6037+165_6037+166del