Canonical Allele Identifier: CA381675816

Gene: SHANK2

Linked Data

• MyVariant Identifiers: chr11:g.70319249C>G (hg19) ; chr11:g.70473144C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70473144C>G , CM000673.2:g.70473144C>G	GRCh38
NC_000011.9:g.70319249C>G , CM000673.1:g.70319249C>G	GRCh37
NC_000011.8:g.69996897C>G	NCBI36
NG_042866.1:g.656653G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.3508G>C	ENSP00000345193.7:p.Gly1170Arg
ENST00000412252.6:c.1053G>C	ENSP00000414876.2:n.1053G>C
ENST00000601538.6:c.5275G>C MANE Select	ENSP00000469689.2:p.Gly1759Arg
ENST00000654939.1:c.2784G>C
ENST00000656230.1:c.4138G>C	ENSP00000499561.1:p.Gly1380Arg
ENST00000659264.1:c.3565G>C	ENSP00000499270.1:p.Gly1189Arg
ENST00000338508.8:c.3511G>C	ENSP00000345193.6:p.Gly1171Arg
ENST00000357171.7:c.*279G>C	ENSP00000349694.4:n.*279G>C
ENST00000409161.5:c.3487G>C	ENSP00000386491.1:p.Gly1163Arg
ENST00000412252.5:c.1051G>C
ENST00000423696.6:c.4138G>C	ENSP00000394536.2:p.Gly1380Arg
ENST00000424924.5:c.3112G>C	ENSP00000402944.1:p.Gly1038Arg
ENST00000449833.6:c.3511G>C	ENSP00000399423.3:p.Gly1171Arg
ENST00000601538.5:c.5275G>C	ENSP00000469689.2:p.Gly1759Arg
ENST00000606715.3:n.2027G>C
NM_012309.4:c.5275G>C	NP_036441.2:p.Gly1759Arg
NM_133266.4:c.3511G>C	NP_573573.2:p.Gly1171Arg
NR_110766.1:n.1129G>C
XM_005277930.2:c.5275G>C	XP_005277987.1:p.Gly1759Arg
XM_005277932.2:c.4138G>C	XP_005277989.1:p.Gly1380Arg
XM_006718478.2:c.5245G>C	XP_006718541.1:p.Gly1749Arg
XM_011544854.1:c.5287G>C	XP_011543156.1:p.Gly1763Arg
XM_011544855.1:c.5266G>C	XP_011543157.1:p.Gly1756Arg
XM_011544856.1:c.5260G>C	XP_011543158.1:p.Gly1754Arg
XM_011544857.1:c.5239G>C	XP_011543159.1:p.Gly1747Arg
XM_011544859.1:c.4150G>C	XP_011543161.1:p.Gly1384Arg
XM_005277932.3:c.4138G>C	XP_005277989.1:p.Gly1380Arg
XM_017017387.1:c.5275G>C	XP_016872876.1:p.Gly1759Arg
XM_017017388.1:c.5275G>C	XP_016872877.1:p.Gly1759Arg
XM_017017389.1:c.5248G>C	XP_016872878.1:p.Gly1750Arg
XM_017017390.1:c.3565G>C	XP_016872879.1:p.Gly1189Arg
NM_133266.5:c.3511G>C	NP_573573.2:p.Gly1171Arg
NR_110766.2:n.1130G>C
NM_001379226.1:c.4138G>C	NP_001366155.1:p.Gly1380Arg
NM_012309.5:c.5275G>C MANE Select	NP_036441.2:p.Gly1759Arg