Canonical Allele Identifier: CA2838010858

Gene: FYN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111873230C>G , CM000668.2:g.111873230C>G	GRCh38
NC_000006.11:g.112194433C>G , CM000668.1:g.112194433C>G	GRCh37
NC_000006.10:g.112301126C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368682.8:c.-385G>C	ENSP00000357671.3:n.-385G>C
ENST00000354650.7:c.-385G>C MANE Select	ENSP00000346671.3:n.-385G>C
ENST00000368678.8:c.-315G>C	ENSP00000357667.4:n.-315G>C
ENST00000484067.6:c.-360-25G>C	ENSP00000428983.1:n.-360-25G>C
ENST00000518295.5:c.-502G>C	ENSP00000428695.1:n.-502G>C
ENST00000523238.5:c.-344G>C	ENSP00000430364.1:n.-344G>C
NM_002037.5:c.-385G>C MANE Select	NP_002028.1:n.-385G>C
XM_005266890.2:c.-385G>C	XP_005266947.1:n.-385G>C
XM_005266892.2:c.-385G>C	XP_005266949.1:n.-385G>C
XM_011535662.1:c.-385G>C	XP_011533964.1:n.-385G>C
XM_011535663.1:c.-344G>C	XP_011533965.1:n.-344G>C
XM_011536304.1:c.499C>G	XP_011534606.1:p.Arg167Gly
XM_024446614.1:c.499C>G	XP_024302382.1:p.Arg167Gly