Canonical Allele Identifier: CA515260659
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159345G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50720917G>C , CM000684.2:g.50720917G>C GRCh38
NC_000022.10:g.51159345G>C , CM000684.1:g.51159345G>C GRCh37
NC_000022.9:g.49506211G>C NCBI36
NG_008607.2:g.51563G>C
NG_070230.1:g.56701G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2685G>C ENSP00000489147.2:p.Val895=
ENST00000414786.7:n.3269G>C
ENST00000445220.7:c.1737G>C ENSP00000489407.2:p.Val579=
ENST00000664402.2:c.1227G>C ENSP00000499475.1:p.Val409=
ENST00000673971.2:c.*1683G>C ENSP00000501192.1:n.*1683G>C
ENST00000445220.6:c.1737G>C ENSP00000489407.2:p.Val579=
ENST00000262795.6:c.2685G>C ENSP00000489147.2:p.Val895=
ENST00000664402.1:c.1227G>C ENSP00000499475.1:p.Val409=
ENST00000673971.1:c.*1683G>C ENSP00000501192.1:n.*1683G>C
ENST00000262795.5:c.3081G>C ENSP00000489147.1:p.Val1027=
ENST00000414786.6:n.3269G>C
ENST00000445220.5:c.3063G>C ENSP00000489407.1:p.Val1021=