Canonical Allele Identifier: CA515266923
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51169372A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50730944A>C , CM000684.2:g.50730944A>C GRCh38
NC_000022.10:g.51169372A>C , CM000684.1:g.51169372A>C GRCh37
NC_000022.9:g.49516238A>C NCBI36
NG_008607.2:g.61590A>C
NG_070230.1:g.66728A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.4456A>C ENSP00000489147.2:p.Lys1486Gln
ENST00000414786.7:n.5040A>C
ENST00000445220.7:c.3508A>C ENSP00000489407.2:p.Lys1170Gln
ENST00000664402.2:c.2998A>C ENSP00000499475.1:p.Lys1000Gln
ENST00000673971.2:c.*3454A>C ENSP00000501192.1:n.*3454A>C
ENST00000445220.6:c.3508A>C ENSP00000489407.2:p.Lys1170Gln
ENST00000262795.6:c.4456A>C ENSP00000489147.2:p.Lys1486Gln
ENST00000659388.1:c.271A>C ENSP00000499632.1:p.Lys91Gln
ENST00000664402.1:c.2998A>C ENSP00000499475.1:p.Lys1000Gln
ENST00000673971.1:c.*3454A>C ENSP00000501192.1:n.*3454A>C
ENST00000262795.5:c.4825A>C ENSP00000489147.1:p.Lys1609Gln
ENST00000414786.6:n.5040A>C
ENST00000445220.5:c.4807A>C ENSP00000489407.1:p.Lys1603Gln