Canonical Allele Identifier: CA2680044034

Gene: FYN

Linked Data

• gnomAD v4: 6-111873097-GGGCGGCGCCGGGGTGTCCCCGGCCCGGCGGCCGAATCCCTCCCTGGCGCGGGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111873104_111873156del , CM000668.2:g.111873104_111873156del	GRCh38
NC_000006.11:g.112194307_112194359del , CM000668.1:g.112194307_112194359del	GRCh37
NC_000006.10:g.112301000_112301052del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368682.8:c.-305_-253del	ENSP00000357671.3:n.-305_-253del
ENST00000354650.7:c.-305_-253del MANE Select	ENSP00000346671.3:n.-305_-253del
ENST00000368678.8:c.-235_-183del	ENSP00000357667.4:n.-235_-183del
ENST00000484067.6:c.-305_-253del	ENSP00000428983.1:n.-305_-253del
ENST00000518295.5:c.-422_-370del	ENSP00000428695.1:n.-422_-370del
ENST00000523238.5:c.-264_-212del	ENSP00000430364.1:n.-264_-212del
NM_002037.5:c.-305_-253del MANE Select	NP_002028.1:n.-305_-253del
XM_005266890.2:c.-305_-253del	XP_005266947.1:n.-305_-253del
XM_005266892.2:c.-305_-253del	XP_005266949.1:n.-305_-253del
XM_011535662.1:c.-305_-253del	XP_011533964.1:n.-305_-253del
XM_011535663.1:c.-264_-212del	XP_011533965.1:n.-264_-212del
XM_011536304.1:c.373_425del	XP_011534606.1:p.Ala125ArgfsTer?
XM_024446614.1:c.373_425del	XP_024302382.1:p.Ala125ArgfsTer?