Canonical Allele Identifier: CA2175492152

Gene: FBN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48445360_48445361delinsTA , CM000677.2:g.48445360_48445361delinsTA	GRCh38
NC_000015.9:g.48737557_48737558delinsTA , CM000677.1:g.48737557_48737558delinsTA	GRCh37
NC_000015.8:g.46524849_46524850delinsTA	NCBI36
NG_008805.2:g.205428_205429delinsTA , LRG_778:g.205428_205429delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.5917+15_5917+16delinsTA	ENSP00000453958.2:n.5917+15_5917+16delinsTA
ENST00000674301.2:c.5917+15_5917+16delinsTA	ENSP00000501333.2:n.5917+15_5917+16delinsTA
ENST00000684448.1:n.4591+15_4591+16delinsTA
ENST00000316623.10:c.5917+15_5917+16delinsTA MANE Select	ENSP00000325527.5:n.5917+15_5917+16delinsTA
ENST00000674301.1:c.916+15_916+16delinsTA	ENSP00000501333.1:n.916+15_916+16delinsTA
ENST00000316623.9:c.5917+15_5917+16delinsTA	ENSP00000325527.5:n.5917+15_5917+16delinsTA
ENST00000537463.6:c.*1680+15_*1680+16delinsTA	ENSP00000440294.2:n.*1680+15_*1680+16delinsTA
ENST00000559133.5:c.1224+15_1224+16delinsTA
ENST00000560820.1:n.37+15_37+16delinsTA
NM_000138.4:c.5917+15_5917+16delinsTA , LRG_778t1:c.5917+15_5917+16delinsTA	NP_000129.3:n.5917+15_5917+16delinsTA
NM_000138.5:c.5917+15_5917+16delinsTA MANE Select	NP_000129.3:n.5917+15_5917+16delinsTA