Canonical Allele Identifier: CA1655020176

Gene: FYN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111661054A= , CM000668.2:g.111661054A=	GRCh38
NC_000006.11:g.111982257A= , CM000668.1:g.111982257A=	GRCh37
NC_000006.10:g.112088950A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368682.8:c.*685T=	ENSP00000357671.3:n.*685T=
ENST00000354650.7:c.*685T= MANE Select	ENSP00000346671.3:n.*685T=
ENST00000368682.7:c.*685T=	ENSP00000357671.3:n.*685T=
ENST00000538466.5:c.*685T=	ENSP00000440646.1:n.*685T=
NM_002037.5:c.*685T= MANE Select	NP_002028.1:n.*685T=
NM_153047.3:c.*685T=	NP_694592.1:n.*685T=
NM_153048.3:c.*685T=	NP_694593.1:n.*685T=
XM_005266890.2:c.*685T=	XP_005266947.1:n.*685T=
XM_005266892.2:c.*685T=	XP_005266949.1:n.*685T=
XM_011535662.1:c.*685T=	XP_011533964.1:n.*685T=
XM_011535663.1:c.*685T=	XP_011533965.1:n.*685T=
XM_011535664.1:c.*685T=	XP_011533966.1:n.*685T=
XM_011535665.1:c.*685T=	XP_011533967.1:n.*685T=
XM_011535666.1:c.*685T=	XP_011533968.1:n.*685T=
XM_011535667.1:c.*685T=	XP_011533969.1:n.*685T=
XM_011535668.1:c.*685T=	XP_011533970.1:n.*685T=
XM_005266890.4:c.*685T=	XP_005266947.1:n.*685T=
XM_005266892.4:c.*685T=	XP_005266949.1:n.*685T=
XM_017010650.1:c.*685T=	XP_016866139.1:n.*685T=
XM_017010651.1:c.*685T=	XP_016866140.1:n.*685T=
XM_017010652.1:c.*685T=	XP_016866141.1:n.*685T=
XM_017010653.1:c.*685T=	XP_016866142.1:n.*685T=
XM_017010654.1:c.*685T=	XP_016866143.1:n.*685T=
NM_001370529.1:c.*685T=	NP_001357458.1:n.*685T=
NM_153047.4:c.*685T=	NP_694592.1:n.*685T=
NM_153048.4:c.*685T=	NP_694593.1:n.*685T=