Canonical Allele Identifier: CA2680043991
Gene: FYN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111873039G>T , CM000668.2:g.111873039G>T GRCh38
NC_000006.11:g.112194242G>T , CM000668.1:g.112194242G>T GRCh37
NC_000006.10:g.112300935G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368682.8:c.-194C>A ENSP00000357671.3:n.-194C>A
ENST00000354650.7:c.-194C>A MANE Select ENSP00000346671.3:n.-194C>A
ENST00000368678.8:c.-124C>A ENSP00000357667.4:n.-124C>A
ENST00000368682.7:c.-194C>A ENSP00000357671.3:n.-194C>A
ENST00000484067.6:c.-194C>A ENSP00000428983.1:n.-194C>A
ENST00000518295.5:c.-311C>A ENSP00000428695.1:n.-311C>A
ENST00000523238.5:c.-153C>A ENSP00000430364.1:n.-153C>A
NM_002037.5:c.-194C>A MANE Select NP_002028.1:n.-194C>A
XM_005266890.2:c.-194C>A XP_005266947.1:n.-194C>A
XM_005266892.2:c.-194C>A XP_005266949.1:n.-194C>A
XM_011535662.1:c.-194C>A XP_011533964.1:n.-194C>A
XM_011535663.1:c.-153C>A XP_011533965.1:n.-153C>A
XM_011536304.1:c.308G>T XP_011534606.1:p.Arg103Leu
XM_005266890.4:c.-194C>A XP_005266947.1:n.-194C>A
XM_005266892.4:c.-194C>A XP_005266949.1:n.-194C>A
XM_017010655.2:c.-194C>A XP_016866144.1:n.-194C>A
XM_024446614.1:c.308G>T XP_024302382.1:p.Arg103Leu
NM_153047.4:c.-194C>A NP_694592.1:n.-194C>A