Canonical Allele Identifier: CA1655112496
Gene: FYN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111873138C= , CM000668.2:g.111873138C= GRCh38
NC_000006.11:g.112194341C= , CM000668.1:g.112194341C= GRCh37
NC_000006.10:g.112301034C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000368682.8:c.-293G= ENSP00000357671.3:n.-293G=
ENST00000354650.7:c.-293G= MANE Select ENSP00000346671.3:n.-293G=
ENST00000368678.8:c.-223G= ENSP00000357667.4:n.-223G=
ENST00000484067.6:c.-293G= ENSP00000428983.1:n.-293G=
ENST00000518295.5:c.-410G= ENSP00000428695.1:n.-410G=
ENST00000523238.5:c.-252G= ENSP00000430364.1:n.-252G=
NM_002037.5:c.-293G= MANE Select NP_002028.1:n.-293G=
XM_005266890.2:c.-293G= XP_005266947.1:n.-293G=
XM_005266892.2:c.-293G= XP_005266949.1:n.-293G=
XM_011535662.1:c.-293G= XP_011533964.1:n.-293G=
XM_011535663.1:c.-252G= XP_011533965.1:n.-252G=
XM_011536304.1:c.407C= XP_011534606.1:p.Ser136=
XM_024446614.1:c.407C= XP_024302382.1:p.Ser136=