Canonical Allele Identifier: CA817275984

Gene: FYN

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111720156T>A , CM000668.2:g.111720156T>A	GRCh38
NC_000006.11:g.112041359T>A , CM000668.1:g.112041359T>A	GRCh37
NC_000006.10:g.112148052T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368682.8:c.-11-94A>T	ENSP00000357671.3:n.-11-94A>T
ENST00000229471.8:c.-11-94A>T	ENSP00000229471.4:n.-11-94A>T
ENST00000354650.7:c.-11-94A>T MANE Select	ENSP00000346671.3:n.-11-94A>T
ENST00000368667.6:c.-11-94A>T	ENSP00000357656.2:n.-11-94A>T
ENST00000368678.8:c.-11-94A>T	ENSP00000357667.4:n.-11-94A>T
ENST00000368682.7:c.-11-94A>T	ENSP00000357671.3:n.-11-94A>T
ENST00000462598.7:c.-11-94A>T	ENSP00000429590.2:n.-11-94A>T
ENST00000462856.6:c.-11-94A>T	ENSP00000427993.1:n.-11-94A>T
ENST00000484067.6:c.-11-94A>T	ENSP00000428983.1:n.-11-94A>T
ENST00000487824.2:c.-11-94A>T	ENSP00000430455.1:n.-11-94A>T
ENST00000517419.5:c.-11-94A>T	ENSP00000429866.1:n.-11-94A>T
ENST00000518295.5:c.-11-94A>T	ENSP00000428695.1:n.-11-94A>T
ENST00000518630.5:c.-11-94A>T	ENSP00000429813.1:n.-11-94A>T
ENST00000520518.5:c.-11-94A>T	ENSP00000429294.1:n.-11-94A>T
ENST00000521062.5:c.-11-94A>T	ENSP00000428042.1:n.-11-94A>T
ENST00000521361.5:n.318-94A>T
ENST00000523238.5:c.-11-94A>T	ENSP00000430364.1:n.-11-94A>T
ENST00000523322.5:n.195-94A>T
ENST00000523570.5:c.-11-94A>T	ENSP00000428045.1:n.-11-94A>T
ENST00000523574.5:c.-11-94A>T	ENSP00000429992.1:n.-11-94A>T
ENST00000524310.5:c.-11-94A>T	ENSP00000428493.1:n.-11-94A>T
NM_002037.5:c.-11-94A>T MANE Select	NP_002028.1:n.-11-94A>T
NM_153048.3:c.-11-94A>T	NP_694593.1:n.-11-94A>T
XM_005266890.2:c.-11-94A>T	XP_005266947.1:n.-11-94A>T
XM_005266892.2:c.-11-94A>T	XP_005266949.1:n.-11-94A>T
XM_011535662.1:c.-11-94A>T	XP_011533964.1:n.-11-94A>T
XM_011535663.1:c.-11-94A>T	XP_011533965.1:n.-11-94A>T
XM_011535664.1:c.-11-94A>T	XP_011533966.1:n.-11-94A>T
XM_011535665.1:c.-11-94A>T	XP_011533967.1:n.-11-94A>T
XM_011535666.1:c.-11-94A>T	XP_011533968.1:n.-11-94A>T
XM_011535667.1:c.-11-94A>T	XP_011533969.1:n.-11-94A>T
XM_011535668.1:c.-11-94A>T	XP_011533970.1:n.-11-94A>T
XM_005266890.4:c.-11-94A>T	XP_005266947.1:n.-11-94A>T
XM_005266892.4:c.-11-94A>T	XP_005266949.1:n.-11-94A>T
XM_017010650.1:c.-11-94A>T	XP_016866139.1:n.-11-94A>T
XM_017010651.1:c.-11-94A>T	XP_016866140.1:n.-11-94A>T
XM_017010652.1:c.-11-94A>T	XP_016866141.1:n.-11-94A>T
XM_017010653.1:c.-11-94A>T	XP_016866142.1:n.-11-94A>T
XM_017010654.1:c.-11-94A>T	XP_016866143.1:n.-11-94A>T
XM_017010655.2:c.-11-94A>T	XP_016866144.1:n.-11-94A>T
NM_001370529.1:c.-11-94A>T	NP_001357458.1:n.-11-94A>T
NM_153047.4:c.-11-94A>T	NP_694592.1:n.-11-94A>T
NM_153048.4:c.-11-94A>T	NP_694593.1:n.-11-94A>T