Canonical Allele Identifier: CA1655112505

Gene: FYN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111873145_111873159delinsGCGGGCGGCGGCCGC , CM000668.2:g.111873145_111873159delinsGCGGGCGGCGGCCGC	GRCh38
NC_000006.11:g.112194348_112194362delinsGCGGGCGGCGGCCGC , CM000668.1:g.112194348_112194362delinsGCGGGCGGCGGCCGC	GRCh37
NC_000006.10:g.112301041_112301055delinsGCGGGCGGCGGCCGC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368682.8:c.-314_-300delinsGCGGCCGCCGCCCGC	ENSP00000357671.3:n.-314_-300delinsGCGGCC...
ENST00000354650.7:c.-314_-300delinsGCGGCCGCCGCCCGC MANE Select	ENSP00000346671.3:n.-314_-300delinsGCGGCC...
ENST00000368678.8:c.-244_-230delinsGCGGCCGCCGCCCGC	ENSP00000357667.4:n.-244_-230delinsGCGGCC...
ENST00000484067.6:c.-314_-300delinsGCGGCCGCCGCCCGC	ENSP00000428983.1:n.-314_-300delinsGCGGCC...
ENST00000518295.5:c.-431_-417delinsGCGGCCGCCGCCCGC	ENSP00000428695.1:n.-431_-417delinsGCGGCC...
ENST00000523238.5:c.-273_-259delinsGCGGCCGCCGCCCGC	ENSP00000430364.1:n.-273_-259delinsGCGGCC...
NM_002037.5:c.-314_-300delinsGCGGCCGCCGCCCGC MANE Select	NP_002028.1:n.-314_-300delinsGCGGCCGCCGCC...
XM_005266890.2:c.-314_-300delinsGCGGCCGCCGCCCGC	XP_005266947.1:n.-314_-300delinsGCGGCCGCC...
XM_005266892.2:c.-314_-300delinsGCGGCCGCCGCCCGC	XP_005266949.1:n.-314_-300delinsGCGGCCGCC...
XM_011535662.1:c.-314_-300delinsGCGGCCGCCGCCCGC	XP_011533964.1:n.-314_-300delinsGCGGCCGCC...
XM_011535663.1:c.-273_-259delinsGCGGCCGCCGCCCGC	XP_011533965.1:n.-273_-259delinsGCGGCCGCC...
XM_011536304.1:c.414_428delinsGCGGGCGGCGGCCGC	XP_011534606.1:p.Ala138=
XM_024446614.1:c.414_428delinsGCGGGCGGCGGCCGC	XP_024302382.1:p.Ala138=