Canonical Allele Identifier: CA12204737
Gene: FYN HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1465061

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111760413G>A , CM000668.2:g.111760413G>A GRCh38
NC_000006.11:g.112081616G>A , CM000668.1:g.112081616G>A GRCh37
NC_000006.10:g.112188309G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_002037.5:c.-12+20153C>T VV MANE Preferred NP_002028.1:p.=
XM_005266890.2:c.-12+20153C>T XP_005266947.1:p.=
XM_005266892.2:c.-12+20153C>T XP_005266949.1:p.=
XM_011535662.1:c.-12+20153C>T XP_011533964.1:p.=
XM_011535663.1:c.-12+20153C>T XP_011533965.1:p.=
XM_011535664.1:c.-12+20153C>T XP_011533966.1:p.=
XM_011535665.1:c.-12+20153C>T XP_011533967.1:p.=
XM_005266890.4:c.-12+20153C>T XP_005266947.1:p.=
XM_005266892.4:c.-12+20153C>T XP_005266949.1:p.=
XM_017010650.1:c.-12+20153C>T XP_016866139.1:p.=
XM_017010651.1:c.-12+20153C>T XP_016866140.1:p.=
XM_017010655.2:c.-12+20153C>T XP_016866144.1:p.=
ENST00000354650.7:c.-12+20153C>T ENSP00000346671.3:p.=
ENST00000368667.6:c.-12+20153C>T ENSP00000357656.2:p.=
ENST00000368678.8:c.-11-40351C>T ENSP00000357667.4:p.=
ENST00000368682.7:c.-12+20153C>T ENSP00000357671.3:p.=
ENST00000462598.7:c.-255-5736C>T ENSP00000429590.2:p.=
ENST00000484067.6:c.-12+20153C>T ENSP00000428983.1:p.=
ENST00000487824.2:c.-12+20153C>T ENSP00000430455.1:p.=
ENST00000518295.5:c.-128-19316C>T ENSP00000428695.1:p.=
ENST00000518630.5:c.-12+20153C>T ENSP00000429813.1:p.=
ENST00000520518.5:c.-124-19320C>T ENSP00000429294.1:p.=
ENST00000521062.5:c.-12+20153C>T ENSP00000428042.1:p.=
ENST00000521361.5:n.317+20153C>T
ENST00000523238.5:c.-12+20153C>T ENSP00000430364.1:p.=
ENST00000523570.5:c.-12+20153C>T ENSP00000428045.1:p.=
ENST00000523574.5:c.-12+20153C>T ENSP00000429992.1:p.=
ENST00000524310.5:c.-12+20153C>T ENSP00000428493.1:p.=