Canonical Allele Identifier: CA381676766

Gene: SHANK2

Linked Data

• MyVariant Identifiers: chr11:g.70319515C>T (hg19) ; chr11:g.70473410C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70473410C>T , CM000673.2:g.70473410C>T	GRCh38
NC_000011.9:g.70319515C>T , CM000673.1:g.70319515C>T	GRCh37
NC_000011.8:g.69997163C>T	NCBI36
NG_042866.1:g.656387G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.3242G>A	ENSP00000345193.7:p.Gly1081Asp
ENST00000412252.6:c.787G>A	ENSP00000414876.2:n.787G>A
ENST00000601538.6:c.5009G>A MANE Select	ENSP00000469689.2:p.Gly1670Asp
ENST00000654939.1:c.2518G>A
ENST00000656230.1:c.3872G>A	ENSP00000499561.1:p.Gly1291Asp
ENST00000659264.1:c.3299G>A	ENSP00000499270.1:p.Gly1100Asp
ENST00000338508.8:c.3245G>A	ENSP00000345193.6:p.Gly1082Asp
ENST00000357171.7:c.*13G>A	ENSP00000349694.4:n.*13G>A
ENST00000409161.5:c.3221G>A	ENSP00000386491.1:p.Gly1074Asp
ENST00000412252.5:c.785G>A
ENST00000423696.6:c.3872G>A	ENSP00000394536.2:p.Gly1291Asp
ENST00000424924.5:c.2846G>A	ENSP00000402944.1:p.Gly949Asp
ENST00000449833.6:c.3245G>A	ENSP00000399423.3:p.Gly1082Asp
ENST00000601538.5:c.5009G>A	ENSP00000469689.2:p.Gly1670Asp
ENST00000606715.3:n.1761G>A
NM_012309.4:c.5009G>A	NP_036441.2:p.Gly1670Asp
NM_133266.4:c.3245G>A	NP_573573.2:p.Gly1082Asp
NR_110766.1:n.863G>A
XM_005277930.2:c.5009G>A	XP_005277987.1:p.Gly1670Asp
XM_005277932.2:c.3872G>A	XP_005277989.1:p.Gly1291Asp
XM_006718478.2:c.4979G>A	XP_006718541.1:p.Gly1660Asp
XM_011544854.1:c.5021G>A	XP_011543156.1:p.Gly1674Asp
XM_011544855.1:c.5000G>A	XP_011543157.1:p.Gly1667Asp
XM_011544856.1:c.4994G>A	XP_011543158.1:p.Gly1665Asp
XM_011544857.1:c.4973G>A	XP_011543159.1:p.Gly1658Asp
XM_011544859.1:c.3884G>A	XP_011543161.1:p.Gly1295Asp
XM_005277932.3:c.3872G>A	XP_005277989.1:p.Gly1291Asp
XM_017017387.1:c.5009G>A	XP_016872876.1:p.Gly1670Asp
XM_017017388.1:c.5009G>A	XP_016872877.1:p.Gly1670Asp
XM_017017389.1:c.4982G>A	XP_016872878.1:p.Gly1661Asp
XM_017017390.1:c.3299G>A	XP_016872879.1:p.Gly1100Asp
NM_133266.5:c.3245G>A	NP_573573.2:p.Gly1082Asp
NR_110766.2:n.864G>A
NM_001379226.1:c.3872G>A	NP_001366155.1:p.Gly1291Asp
NM_012309.5:c.5009G>A MANE Select	NP_036441.2:p.Gly1670Asp