Canonical Allele Identifier: CA1655112507
Gene: FYN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111873147G= , CM000668.2:g.111873147G= GRCh38
NC_000006.11:g.112194350G= , CM000668.1:g.112194350G= GRCh37
NC_000006.10:g.112301043G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000368682.8:c.-302C= ENSP00000357671.3:n.-302C=
ENST00000354650.7:c.-302C= MANE Select ENSP00000346671.3:n.-302C=
ENST00000368678.8:c.-232C= ENSP00000357667.4:n.-232C=
ENST00000484067.6:c.-302C= ENSP00000428983.1:n.-302C=
ENST00000518295.5:c.-419C= ENSP00000428695.1:n.-419C=
ENST00000523238.5:c.-261C= ENSP00000430364.1:n.-261C=
NM_002037.5:c.-302C= MANE Select NP_002028.1:n.-302C=
XM_005266890.2:c.-302C= XP_005266947.1:n.-302C=
XM_005266892.2:c.-302C= XP_005266949.1:n.-302C=
XM_011535662.1:c.-302C= XP_011533964.1:n.-302C=
XM_011535663.1:c.-261C= XP_011533965.1:n.-261C=
XM_011536304.1:c.416G= XP_011534606.1:p.Arg139=
XM_024446614.1:c.416G= XP_024302382.1:p.Arg139=