Canonical Allele Identifier: CA2680044110

Gene: FYN

Linked Data

• gnomAD v4: 6-111873239-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111873239G>T , CM000668.2:g.111873239G>T	GRCh38
NC_000006.11:g.112194442G>T , CM000668.1:g.112194442G>T	GRCh37
NC_000006.10:g.112301135G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368682.8:c.-394C>A	ENSP00000357671.3:n.-394C>A
ENST00000354650.7:c.-394C>A MANE Select	ENSP00000346671.3:n.-394C>A
ENST00000368678.8:c.-324C>A	ENSP00000357667.4:n.-324C>A
ENST00000484067.6:c.-361+31C>A	ENSP00000428983.1:n.-361+31C>A
ENST00000518295.5:c.-511C>A	ENSP00000428695.1:n.-511C>A
ENST00000523238.5:c.-353C>A	ENSP00000430364.1:n.-353C>A
NM_002037.5:c.-394C>A MANE Select	NP_002028.1:n.-394C>A
XM_005266890.2:c.-394C>A	XP_005266947.1:n.-394C>A
XM_005266892.2:c.-394C>A	XP_005266949.1:n.-394C>A
XM_011535662.1:c.-394C>A	XP_011533964.1:n.-394C>A
XM_011535663.1:c.-353C>A	XP_011533965.1:n.-353C>A
XM_011536304.1:c.508G>T	XP_011534606.1:p.Ala170Ser
XM_024446614.1:c.508G>T	XP_024302382.1:p.Ala170Ser