Canonical Allele Identifier: CA569738154

Gene: FYN

Linked Data

• dbSNP Id: rs1340516825
• gnomAD v2: 6-112194344-T-TGGCGCGGGCGGCGGCCGCCGGGCGGTGC
• gnomAD v3: 6-111873141-T-TGGCGCGGGCGGCGGCCGCCGGGCGGTGC
• gnomAD v4: 6-111873141-T-TGGCGCGGGCGGCGGCCGCCGGGCGGTGC
• MyVariant Identifiers: chr6:g.112194372_112194373insGGCGCGGGCGGCGGCCGCCGGGCGGTGC (hg19) ; chr6:g.112194344_112194345insGGCGCGGGCGGCGGCCGCCGGGCGGTGC (hg19) ; chr6:g.111873169_111873170insGGCGCGGGCGGCGGCCGCCGGGCGGTGC (hg38) ; chr6:g.111873141_111873142insGGCGCGGGCGGCGGCCGCCGGGCGGTGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111873157_111873184dup , CM000668.2:g.111873157_111873184dup	GRCh38
NC_000006.11:g.112194360_112194387dup , CM000668.1:g.112194360_112194387dup	GRCh37
NC_000006.10:g.112301053_112301080dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368682.8:c.-324_-297dup	ENSP00000357671.3:n.-324_-297dup
ENST00000354650.7:c.-324_-297dup MANE Select	ENSP00000346671.3:n.-324_-297dup
ENST00000368678.8:c.-254_-227dup	ENSP00000357667.4:n.-254_-227dup
ENST00000484067.6:c.-324_-297dup	ENSP00000428983.1:n.-324_-297dup
ENST00000518295.5:c.-441_-414dup	ENSP00000428695.1:n.-441_-414dup
ENST00000523238.5:c.-283_-256dup	ENSP00000430364.1:n.-283_-256dup
NM_002037.5:c.-324_-297dup MANE Select	NP_002028.1:n.-324_-297dup
XM_005266890.2:c.-324_-297dup	XP_005266947.1:n.-324_-297dup
XM_005266892.2:c.-324_-297dup	XP_005266949.1:n.-324_-297dup
XM_011535662.1:c.-324_-297dup	XP_011533964.1:n.-324_-297dup
XM_011535663.1:c.-283_-256dup	XP_011533965.1:n.-283_-256dup
XM_011536304.1:c.426_453dup	XP_011534606.1:p.Phe152ArgfsTer?
XM_024446614.1:c.426_453dup	XP_024302382.1:p.Phe152ArgfsTer?