Canonical Allele Identifier: CA2772638089

Gene: FYN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111760230C>A , CM000668.2:g.111760230C>A	GRCh38
NC_000006.11:g.112081433C>A , CM000668.1:g.112081433C>A	GRCh37
NC_000006.10:g.112188126C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368682.8:c.-12+20336G>T	ENSP00000357671.3:n.-12+20336G>T
ENST00000354650.7:c.-12+20336G>T MANE Select	ENSP00000346671.3:n.-12+20336G>T
ENST00000368667.6:c.-12+20336G>T	ENSP00000357656.2:n.-12+20336G>T
ENST00000368678.8:c.-11-40168G>T	ENSP00000357667.4:n.-11-40168G>T
ENST00000368682.7:c.-12+20336G>T	ENSP00000357671.3:n.-12+20336G>T
ENST00000462598.7:c.-255-5553G>T	ENSP00000429590.2:n.-255-5553G>T
ENST00000484067.6:c.-12+20336G>T	ENSP00000428983.1:n.-12+20336G>T
ENST00000487824.2:c.-12+20336G>T	ENSP00000430455.1:n.-12+20336G>T
ENST00000518295.5:c.-128-19133G>T	ENSP00000428695.1:n.-128-19133G>T
ENST00000518630.5:c.-12+20336G>T	ENSP00000429813.1:n.-12+20336G>T
ENST00000520518.5:c.-124-19137G>T	ENSP00000429294.1:n.-124-19137G>T
ENST00000521062.5:c.-12+20336G>T	ENSP00000428042.1:n.-12+20336G>T
ENST00000521361.5:n.317+20336G>T
ENST00000523238.5:c.-12+20336G>T	ENSP00000430364.1:n.-12+20336G>T
ENST00000523570.5:c.-12+20336G>T	ENSP00000428045.1:n.-12+20336G>T
ENST00000523574.5:c.-12+20336G>T	ENSP00000429992.1:n.-12+20336G>T
ENST00000524310.5:c.-12+20336G>T	ENSP00000428493.1:n.-12+20336G>T
NM_002037.5:c.-12+20336G>T MANE Select	NP_002028.1:n.-12+20336G>T
XM_005266890.2:c.-12+20336G>T	XP_005266947.1:n.-12+20336G>T
XM_005266892.2:c.-12+20336G>T	XP_005266949.1:n.-12+20336G>T
XM_011535662.1:c.-12+20336G>T	XP_011533964.1:n.-12+20336G>T
XM_011535663.1:c.-12+20336G>T	XP_011533965.1:n.-12+20336G>T
XM_011535664.1:c.-12+20336G>T	XP_011533966.1:n.-12+20336G>T
XM_011535665.1:c.-12+20336G>T	XP_011533967.1:n.-12+20336G>T
XM_005266890.4:c.-12+20336G>T	XP_005266947.1:n.-12+20336G>T
XM_005266892.4:c.-12+20336G>T	XP_005266949.1:n.-12+20336G>T
XM_017010650.1:c.-12+20336G>T	XP_016866139.1:n.-12+20336G>T
XM_017010651.1:c.-12+20336G>T	XP_016866140.1:n.-12+20336G>T
XM_017010655.2:c.-12+20336G>T	XP_016866144.1:n.-12+20336G>T
NM_153047.4:c.-12+20336G>T	NP_694592.1:n.-12+20336G>T