Canonical Allele Identifier: CA2672441503

Gene: FGB

Linked Data

• gnomAD v4: 4-154569701-C-CCTCATGGATGGAGCATCTCAG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569704_154569724dup , CM000666.2:g.154569704_154569724dup	GRCh38
NC_000004.11:g.155490856_155490876dup , CM000666.1:g.155490856_155490876dup	GRCh37
NC_000004.10:g.155710306_155710326dup	NCBI36
NG_008833.1:g.11725_11745dup , LRG_558:g.11725_11745dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000302068.9:c.1149_1169dup MANE Select	ENSP00000306099.4:p.Leu390_Met391insMetAs...
ENST00000302068.8:c.1149_1169dup	ENSP00000306099.4:p.Leu390_Met391insMetAs...
ENST00000502545.5:n.939+397_939+417dup
ENST00000509493.1:c.492_512dup	ENSP00000426757.1:p.Leu171_Met172insMetAs...
NM_001184741.1:c.972_992dup	NP_001171670.1:p.Leu331_Met332insMetAspGl...
NM_005141.4:c.1149_1169dup , LRG_558t1:c.1149_1169dup	NP_005132.2:p.Leu390_Met391insMetAspGlyAl...
NM_001382759.1:c.1017_1037dup	NP_001369688.1:p.Leu346_Met347insMetAspGl...
NM_001382760.1:c.1149_1169dup	NP_001369689.1:p.Leu390_Met391insMetAspGl...
NM_001382761.1:c.1149_1169dup	NP_001369690.1:p.Leu390_Met391insMetAspGl...
NM_001382762.1:c.849_869dup	NP_001369691.1:p.Leu290_Met291insMetAspGl...
NM_001382763.1:c.1140_1160dup	NP_001369692.1:p.Leu387_Met388insMetAspGl...
NM_001382764.1:c.1081-69_1081-49dup	NP_001369693.1:n.1081-69_1081-49dup
NM_001382765.1:c.1149_1169dup	NP_001369694.1:p.Leu390_Met391insMetAspGl...
NM_005141.5:c.1149_1169dup MANE Select	NP_005132.2:p.Leu390_Met391insMetAspGlyAl...