Canonical Allele Identifier: CA515264878
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51160671G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50722243G>C , CM000684.2:g.50722243G>C GRCh38
NC_000022.10:g.51160671G>C , CM000684.1:g.51160671G>C GRCh37
NC_000022.9:g.49507537G>C NCBI36
NG_008607.2:g.52889G>C
NG_070230.1:g.58027G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.4011G>C ENSP00000489147.2:p.Arg1337Ser
ENST00000414786.7:n.4595G>C
ENST00000445220.7:c.3063G>C ENSP00000489407.2:p.Arg1021Ser
ENST00000664402.2:c.2553G>C ENSP00000499475.1:p.Arg851Ser
ENST00000673971.2:c.*3009G>C ENSP00000501192.1:n.*3009G>C
ENST00000445220.6:c.3063G>C ENSP00000489407.2:p.Arg1021Ser
ENST00000262795.6:c.4011G>C ENSP00000489147.2:p.Arg1337Ser
ENST00000664402.1:c.2553G>C ENSP00000499475.1:p.Arg851Ser
ENST00000673971.1:c.*3009G>C ENSP00000501192.1:n.*3009G>C
ENST00000262795.5:c.4407G>C ENSP00000489147.1:p.Arg1469Ser
ENST00000414786.6:n.4595G>C
ENST00000445220.5:c.4389G>C ENSP00000489407.1:p.Arg1463Ser