Canonical Allele Identifier: CA2675121757

Gene: FBN2

Linked Data

• gnomAD v4: 5-128528014-TTATAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128528019_128528023del , CM000667.2:g.128528019_128528023del	GRCh38
NC_000005.9:g.127863712_127863716del , CM000667.1:g.127863712_127863716del	GRCh37
NC_000005.8:g.127891611_127891615del	NCBI36
NG_008750.1:g.15024_15028del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508053.6:c.437-52_437-48del	ENSP00000424571.2:n.437-52_437-48del
ENST00000703787.1:n.144-52_144-48del
ENST00000262464.9:c.437-52_437-48del MANE Select	ENSP00000262464.4:n.437-52_437-48del
ENST00000262464.8:c.437-52_437-48del	ENSP00000262464.4:n.437-52_437-48del
ENST00000502468.5:c.437-52_437-48del	ENSP00000424753.1:n.437-52_437-48del
ENST00000508053.5:c.437-52_437-48del	ENSP00000424571.1:n.437-52_437-48del
ENST00000508989.5:c.338-52_338-48del	ENSP00000425596.1:n.338-52_338-48del
ENST00000514742.1:n.1057-52_1057-48del
ENST00000619499.4:c.437-52_437-48del	ENSP00000482132.1:n.437-52_437-48del
ENST00000620257.1:c.437-52_437-48del	ENSP00000479157.1:n.437-52_437-48del
NM_001999.3:c.437-52_437-48del	NP_001990.2:n.437-52_437-48del
XM_017009228.2:c.437-52_437-48del	XP_016864717.1:n.437-52_437-48del
NM_001999.4:c.437-52_437-48del MANE Select	NP_001990.2:n.437-52_437-48del