Canonical Allele Identifier: CA1655062879
Gene: FYN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111760251G= , CM000668.2:g.111760251G= GRCh38
NC_000006.11:g.112081454G= , CM000668.1:g.112081454G= GRCh37
NC_000006.10:g.112188147G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368682.8:c.-12+20315C= ENSP00000357671.3:n.-12+20315C=
ENST00000354650.7:c.-12+20315C= MANE Select ENSP00000346671.3:n.-12+20315C=
ENST00000368667.6:c.-12+20315C= ENSP00000357656.2:n.-12+20315C=
ENST00000368678.8:c.-11-40189C= ENSP00000357667.4:n.-11-40189C=
ENST00000368682.7:c.-12+20315C= ENSP00000357671.3:n.-12+20315C=
ENST00000462598.7:c.-255-5574C= ENSP00000429590.2:n.-255-5574C=
ENST00000484067.6:c.-12+20315C= ENSP00000428983.1:n.-12+20315C=
ENST00000487824.2:c.-12+20315C= ENSP00000430455.1:n.-12+20315C=
ENST00000518295.5:c.-128-19154C= ENSP00000428695.1:n.-128-19154C=
ENST00000518630.5:c.-12+20315C= ENSP00000429813.1:n.-12+20315C=
ENST00000520518.5:c.-124-19158C= ENSP00000429294.1:n.-124-19158C=
ENST00000521062.5:c.-12+20315C= ENSP00000428042.1:n.-12+20315C=
ENST00000521361.5:n.317+20315C=
ENST00000523238.5:c.-12+20315C= ENSP00000430364.1:n.-12+20315C=
ENST00000523570.5:c.-12+20315C= ENSP00000428045.1:n.-12+20315C=
ENST00000523574.5:c.-12+20315C= ENSP00000429992.1:n.-12+20315C=
ENST00000524310.5:c.-12+20315C= ENSP00000428493.1:n.-12+20315C=
NM_002037.5:c.-12+20315C= MANE Select NP_002028.1:n.-12+20315C=
XM_005266890.2:c.-12+20315C= XP_005266947.1:n.-12+20315C=
XM_005266892.2:c.-12+20315C= XP_005266949.1:n.-12+20315C=
XM_011535662.1:c.-12+20315C= XP_011533964.1:n.-12+20315C=
XM_011535663.1:c.-12+20315C= XP_011533965.1:n.-12+20315C=
XM_011535664.1:c.-12+20315C= XP_011533966.1:n.-12+20315C=
XM_011535665.1:c.-12+20315C= XP_011533967.1:n.-12+20315C=
XM_005266890.4:c.-12+20315C= XP_005266947.1:n.-12+20315C=
XM_005266892.4:c.-12+20315C= XP_005266949.1:n.-12+20315C=
XM_017010650.1:c.-12+20315C= XP_016866139.1:n.-12+20315C=
XM_017010651.1:c.-12+20315C= XP_016866140.1:n.-12+20315C=
XM_017010655.2:c.-12+20315C= XP_016866144.1:n.-12+20315C=
NM_153047.4:c.-12+20315C= NP_694592.1:n.-12+20315C=