Canonical Allele Identifier: CA12303121

Gene: FYN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111801023C>T , CM000668.2:g.111801023C>T	GRCh38
NC_000006.11:g.112122226C>T , CM000668.1:g.112122226C>T	GRCh37
NC_000006.10:g.112228919C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002037.5:c.-81-20388G>A MANE Select	NP_002028.1:n.-81-20388G>A
ENST00000354650.7:c.-81-20388G>A MANE Select	ENSP00000346671.3:n.-81-20388G>A
NM_153047.4:c.-81-20388G>A	NP_694592.1:n.-81-20388G>A
ENST00000368678.8:c.-12+45566G>A	ENSP00000357667.4:n.-12+45566G>A
ENST00000368682.7:c.-81-20388G>A	ENSP00000357671.3:n.-81-20388G>A
ENST00000368682.8:c.-81-20388G>A	ENSP00000357671.3:n.-81-20388G>A
ENST00000484067.6:c.-81-20388G>A	ENSP00000428983.1:n.-81-20388G>A
ENST00000487824.2:c.-82+12869G>A	ENSP00000430455.1:n.-82+12869G>A
ENST00000518295.5:c.-198-20388G>A	ENSP00000428695.1:n.-198-20388G>A
ENST00000518630.5:c.-81-20388G>A	ENSP00000429813.1:n.-81-20388G>A
ENST00000520518.5:c.-194-20388G>A	ENSP00000429294.1:n.-194-20388G>A
ENST00000521062.5:c.-82+18837G>A	ENSP00000428042.1:n.-82+18837G>A
ENST00000521361.5:n.247+17592G>A
ENST00000523238.5:c.-81-20388G>A	ENSP00000430364.1:n.-81-20388G>A
ENST00000523570.5:c.-81-20388G>A	ENSP00000428045.1:n.-81-20388G>A
XM_005266890.2:c.-81-20388G>A	XP_005266947.1:n.-81-20388G>A
XM_005266890.4:c.-81-20388G>A	XP_005266947.1:n.-81-20388G>A
XM_005266892.2:c.-81-20388G>A	XP_005266949.1:n.-81-20388G>A
XM_005266892.4:c.-81-20388G>A	XP_005266949.1:n.-81-20388G>A
XM_011535662.1:c.-81-20388G>A	XP_011533964.1:n.-81-20388G>A
XM_011535663.1:c.-81-20388G>A	XP_011533965.1:n.-81-20388G>A
XM_011535665.1:c.-81-20388G>A	XP_011533967.1:n.-81-20388G>A
XM_017010651.1:c.-81-20388G>A	XP_016866140.1:n.-81-20388G>A
XM_017010655.2:c.-81-20388G>A	XP_016866144.1:n.-81-20388G>A