Canonical Allele Identifier: CA515261281
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159573C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721145C>G , CM000684.2:g.50721145C>G GRCh38
NC_000022.10:g.51159573C>G , CM000684.1:g.51159573C>G GRCh37
NC_000022.9:g.49506439C>G NCBI36
NG_008607.2:g.51791C>G
NG_070230.1:g.56929C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.2913C>G ENSP00000489147.2:p.Pro971=
ENST00000414786.7:n.3497C>G
ENST00000445220.7:c.1965C>G ENSP00000489407.2:p.Pro655=
ENST00000664402.2:c.1455C>G ENSP00000499475.1:p.Pro485=
ENST00000673971.2:c.*1911C>G ENSP00000501192.1:n.*1911C>G
ENST00000445220.6:c.1965C>G ENSP00000489407.2:p.Pro655=
ENST00000262795.6:c.2913C>G ENSP00000489147.2:p.Pro971=
ENST00000664402.1:c.1455C>G ENSP00000499475.1:p.Pro485=
ENST00000673971.1:c.*1911C>G ENSP00000501192.1:n.*1911C>G
ENST00000262795.5:c.3309C>G ENSP00000489147.1:p.Pro1103=
ENST00000414786.6:n.3497C>G
ENST00000445220.5:c.3291C>G ENSP00000489407.1:p.Pro1097=