Canonical Allele Identifier: CA381675398

Gene: SHANK2

Linked Data

• MyVariant Identifiers: chr11:g.70319192A>C (hg19) ; chr11:g.70473087A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70473087A>C , CM000673.2:g.70473087A>C	GRCh38
NC_000011.9:g.70319192A>C , CM000673.1:g.70319192A>C	GRCh37
NC_000011.8:g.69996840A>C	NCBI36
NG_042866.1:g.656710T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.3565T>G	ENSP00000345193.7:p.Phe1189Val
ENST00000412252.6:c.1110T>G	ENSP00000414876.2:n.1110T>G
ENST00000601538.6:c.5332T>G MANE Select	ENSP00000469689.2:p.Phe1778Val
ENST00000654939.1:c.2841T>G
ENST00000656230.1:c.4195T>G	ENSP00000499561.1:p.Phe1399Val
ENST00000659264.1:c.3622T>G	ENSP00000499270.1:p.Phe1208Val
ENST00000338508.8:c.3568T>G	ENSP00000345193.6:p.Phe1190Val
ENST00000357171.7:c.*336T>G	ENSP00000349694.4:n.*336T>G
ENST00000409161.5:c.3544T>G	ENSP00000386491.1:p.Phe1182Val
ENST00000412252.5:c.1108T>G
ENST00000423696.6:c.4195T>G	ENSP00000394536.2:p.Phe1399Val
ENST00000424924.5:c.3169T>G	ENSP00000402944.1:p.Phe1057Val
ENST00000449833.6:c.3568T>G	ENSP00000399423.3:p.Phe1190Val
ENST00000601538.5:c.5332T>G	ENSP00000469689.2:p.Phe1778Val
ENST00000606715.3:n.2084T>G
NM_012309.4:c.5332T>G	NP_036441.2:p.Phe1778Val
NM_133266.4:c.3568T>G	NP_573573.2:p.Phe1190Val
NR_110766.1:n.1186T>G
XM_005277930.2:c.5332T>G	XP_005277987.1:p.Phe1778Val
XM_005277932.2:c.4195T>G	XP_005277989.1:p.Phe1399Val
XM_006718478.2:c.5302T>G	XP_006718541.1:p.Phe1768Val
XM_011544854.1:c.5344T>G	XP_011543156.1:p.Phe1782Val
XM_011544855.1:c.5323T>G	XP_011543157.1:p.Phe1775Val
XM_011544856.1:c.5317T>G	XP_011543158.1:p.Phe1773Val
XM_011544857.1:c.5296T>G	XP_011543159.1:p.Phe1766Val
XM_011544859.1:c.4207T>G	XP_011543161.1:p.Phe1403Val
XM_005277932.3:c.4195T>G	XP_005277989.1:p.Phe1399Val
XM_017017387.1:c.5332T>G	XP_016872876.1:p.Phe1778Val
XM_017017388.1:c.5332T>G	XP_016872877.1:p.Phe1778Val
XM_017017389.1:c.5305T>G	XP_016872878.1:p.Phe1769Val
XM_017017390.1:c.3622T>G	XP_016872879.1:p.Phe1208Val
NM_133266.5:c.3568T>G	NP_573573.2:p.Phe1190Val
NR_110766.2:n.1187T>G
NM_001379226.1:c.4195T>G	NP_001366155.1:p.Phe1399Val
NM_012309.5:c.5332T>G MANE Select	NP_036441.2:p.Phe1778Val