Canonical Allele Identifier: CA1655112431

Gene: FYN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111873040_111873041delinsGC , CM000668.2:g.111873040_111873041delinsGC	GRCh38
NC_000006.11:g.112194243_112194244delinsGC , CM000668.1:g.112194243_112194244delinsGC	GRCh37
NC_000006.10:g.112300936_112300937delinsGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368682.8:c.-196_-195delinsGC	ENSP00000357671.3:n.-196_-195delinsGC
ENST00000354650.7:c.-196_-195delinsGC MANE Select	ENSP00000346671.3:n.-196_-195delinsGC
ENST00000368678.8:c.-126_-125delinsGC	ENSP00000357667.4:n.-126_-125delinsGC
ENST00000368682.7:c.-196_-195delinsGC	ENSP00000357671.3:n.-196_-195delinsGC
ENST00000484067.6:c.-196_-195delinsGC	ENSP00000428983.1:n.-196_-195delinsGC
ENST00000518295.5:c.-313_-312delinsGC	ENSP00000428695.1:n.-313_-312delinsGC
ENST00000523238.5:c.-155_-154delinsGC	ENSP00000430364.1:n.-155_-154delinsGC
NM_002037.5:c.-196_-195delinsGC MANE Select	NP_002028.1:n.-196_-195delinsGC
XM_005266890.2:c.-196_-195delinsGC	XP_005266947.1:n.-196_-195delinsGC
XM_005266892.2:c.-196_-195delinsGC	XP_005266949.1:n.-196_-195delinsGC
XM_011535662.1:c.-196_-195delinsGC	XP_011533964.1:n.-196_-195delinsGC
XM_011535663.1:c.-155_-154delinsGC	XP_011533965.1:n.-155_-154delinsGC
XM_011536304.1:c.309_310delinsGC	XP_011534606.1:p.Arg103=
XM_005266890.4:c.-196_-195delinsGC	XP_005266947.1:n.-196_-195delinsGC
XM_005266892.4:c.-196_-195delinsGC	XP_005266949.1:n.-196_-195delinsGC
XM_017010655.2:c.-196_-195delinsGC	XP_016866144.1:n.-196_-195delinsGC
XM_024446614.1:c.309_310delinsGC	XP_024302382.1:p.Arg103=
NM_153047.4:c.-196_-195delinsGC	NP_694592.1:n.-196_-195delinsGC