Canonical Allele Identifier: CA381675959

Gene: SHANK2

Linked Data

• ClinVar Variation Id: 2663437
• ClinVar RCV Id: RCV003442625
• MyVariant Identifiers: chr11:g.70319276C>T (hg19) ; chr11:g.70473171C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70473171C>T , CM000673.2:g.70473171C>T	GRCh38
NC_000011.9:g.70319276C>T , CM000673.1:g.70319276C>T	GRCh37
NC_000011.8:g.69996924C>T	NCBI36
NG_042866.1:g.656626G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.3481G>A	ENSP00000345193.7:p.Gly1161Arg
ENST00000412252.6:c.1026G>A	ENSP00000414876.2:n.1026G>A
ENST00000601538.6:c.5248G>A MANE Select	ENSP00000469689.2:p.Gly1750Arg
ENST00000654939.1:c.2757G>A
ENST00000656230.1:c.4111G>A	ENSP00000499561.1:p.Gly1371Arg
ENST00000659264.1:c.3538G>A	ENSP00000499270.1:p.Gly1180Arg
ENST00000338508.8:c.3484G>A	ENSP00000345193.6:p.Gly1162Arg
ENST00000357171.7:c.*252G>A	ENSP00000349694.4:n.*252G>A
ENST00000409161.5:c.3460G>A	ENSP00000386491.1:p.Gly1154Arg
ENST00000412252.5:c.1024G>A
ENST00000423696.6:c.4111G>A	ENSP00000394536.2:p.Gly1371Arg
ENST00000424924.5:c.3085G>A	ENSP00000402944.1:p.Gly1029Arg
ENST00000449833.6:c.3484G>A	ENSP00000399423.3:p.Gly1162Arg
ENST00000601538.5:c.5248G>A	ENSP00000469689.2:p.Gly1750Arg
ENST00000606715.3:n.2000G>A
NM_012309.4:c.5248G>A	NP_036441.2:p.Gly1750Arg
NM_133266.4:c.3484G>A	NP_573573.2:p.Gly1162Arg
NR_110766.1:n.1102G>A
XM_005277930.2:c.5248G>A	XP_005277987.1:p.Gly1750Arg
XM_005277932.2:c.4111G>A	XP_005277989.1:p.Gly1371Arg
XM_006718478.2:c.5218G>A	XP_006718541.1:p.Gly1740Arg
XM_011544854.1:c.5260G>A	XP_011543156.1:p.Gly1754Arg
XM_011544855.1:c.5239G>A	XP_011543157.1:p.Gly1747Arg
XM_011544856.1:c.5233G>A	XP_011543158.1:p.Gly1745Arg
XM_011544857.1:c.5212G>A	XP_011543159.1:p.Gly1738Arg
XM_011544859.1:c.4123G>A	XP_011543161.1:p.Gly1375Arg
XM_005277932.3:c.4111G>A	XP_005277989.1:p.Gly1371Arg
XM_017017387.1:c.5248G>A	XP_016872876.1:p.Gly1750Arg
XM_017017388.1:c.5248G>A	XP_016872877.1:p.Gly1750Arg
XM_017017389.1:c.5221G>A	XP_016872878.1:p.Gly1741Arg
XM_017017390.1:c.3538G>A	XP_016872879.1:p.Gly1180Arg
NM_133266.5:c.3484G>A	NP_573573.2:p.Gly1162Arg
NR_110766.2:n.1103G>A
NM_001379226.1:c.4111G>A	NP_001366155.1:p.Gly1371Arg
NM_012309.5:c.5248G>A MANE Select	NP_036441.2:p.Gly1750Arg