Canonical Allele Identifier: CA515261130
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159518T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721090T>C , CM000684.2:g.50721090T>C GRCh38
NC_000022.10:g.51159518T>C , CM000684.1:g.51159518T>C GRCh37
NC_000022.9:g.49506384T>C NCBI36
NG_008607.2:g.51736T>C
NG_070230.1:g.56874T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000262795.7:c.2858T>C ENSP00000489147.2:p.Leu953Pro
ENST00000414786.7:n.3442T>C
ENST00000445220.7:c.1910T>C ENSP00000489407.2:p.Leu637Pro
ENST00000664402.2:c.1400T>C ENSP00000499475.1:p.Leu467Pro
ENST00000673971.2:c.*1856T>C ENSP00000501192.1:n.*1856T>C
ENST00000445220.6:c.1910T>C ENSP00000489407.2:p.Leu637Pro
ENST00000262795.6:c.2858T>C ENSP00000489147.2:p.Leu953Pro
ENST00000664402.1:c.1400T>C ENSP00000499475.1:p.Leu467Pro
ENST00000673971.1:c.*1856T>C ENSP00000501192.1:n.*1856T>C
ENST00000262795.5:c.3254T>C ENSP00000489147.1:p.Leu1085Pro
ENST00000414786.6:n.3442T>C
ENST00000445220.5:c.3236T>C ENSP00000489407.1:p.Leu1079Pro