Canonical Allele Identifier: CA515255038
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51136060C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50697632C>G , CM000684.2:g.50697632C>G GRCh38
NC_000022.10:g.51136060C>G , CM000684.1:g.51136060C>G GRCh37
NC_000022.9:g.49482926C>G NCBI36
NG_008607.2:g.28278C>G
NG_070230.1:g.33497C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.1016C>G ENSP00000489147.2:p.Pro339Arg
ENST00000414786.7:n.1600C>G
ENST00000445220.7:c.68C>G ENSP00000489407.2:p.Pro23Arg
ENST00000673971.2:c.1373C>G ENSP00000501192.1:p.Pro458Arg
ENST00000445220.6:c.68C>G ENSP00000489407.2:p.Pro23Arg
ENST00000262795.6:c.1016C>G ENSP00000489147.2:p.Pro339Arg
ENST00000673971.1:c.1373C>G ENSP00000501192.1:p.Pro458Arg
ENST00000673995.1:c.69C>G
ENST00000262795.5:c.1412C>G ENSP00000489147.1:p.Pro471Arg
ENST00000414786.6:n.1600C>G
ENST00000445220.5:c.1394C>G ENSP00000489407.1:p.Pro465Arg