Canonical Allele Identifier: CA2525321451

Gene: FYN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111873137T>G , CM000668.2:g.111873137T>G	GRCh38
NC_000006.11:g.112194340T>G , CM000668.1:g.112194340T>G	GRCh37
NC_000006.10:g.112301033T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368682.8:c.-292A>C	ENSP00000357671.3:n.-292A>C
ENST00000354650.7:c.-292A>C MANE Select	ENSP00000346671.3:n.-292A>C
ENST00000368678.8:c.-222A>C	ENSP00000357667.4:n.-222A>C
ENST00000484067.6:c.-292A>C	ENSP00000428983.1:n.-292A>C
ENST00000518295.5:c.-409A>C	ENSP00000428695.1:n.-409A>C
ENST00000523238.5:c.-251A>C	ENSP00000430364.1:n.-251A>C
NM_002037.5:c.-292A>C MANE Select	NP_002028.1:n.-292A>C
XM_005266890.2:c.-292A>C	XP_005266947.1:n.-292A>C
XM_005266892.2:c.-292A>C	XP_005266949.1:n.-292A>C
XM_011535662.1:c.-292A>C	XP_011533964.1:n.-292A>C
XM_011535663.1:c.-251A>C	XP_011533965.1:n.-251A>C
XM_011536304.1:c.406T>G	XP_011534606.1:p.Ser136Ala
XM_024446614.1:c.406T>G	XP_024302382.1:p.Ser136Ala