Canonical Allele Identifier: CA381675413

Gene: SHANK2

Linked Data

• MyVariant Identifiers: chr11:g.70319194G>C (hg19) ; chr11:g.70473089G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70473089G>C , CM000673.2:g.70473089G>C	GRCh38
NC_000011.9:g.70319194G>C , CM000673.1:g.70319194G>C	GRCh37
NC_000011.8:g.69996842G>C	NCBI36
NG_042866.1:g.656708C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.3563C>G	ENSP00000345193.7:p.Pro1188Arg
ENST00000412252.6:c.1108C>G	ENSP00000414876.2:n.1108C>G
ENST00000601538.6:c.5330C>G MANE Select	ENSP00000469689.2:p.Pro1777Arg
ENST00000654939.1:c.2839C>G
ENST00000656230.1:c.4193C>G	ENSP00000499561.1:p.Pro1398Arg
ENST00000659264.1:c.3620C>G	ENSP00000499270.1:p.Pro1207Arg
ENST00000338508.8:c.3566C>G	ENSP00000345193.6:p.Pro1189Arg
ENST00000357171.7:c.*334C>G	ENSP00000349694.4:n.*334C>G
ENST00000409161.5:c.3542C>G	ENSP00000386491.1:p.Pro1181Arg
ENST00000412252.5:c.1106C>G
ENST00000423696.6:c.4193C>G	ENSP00000394536.2:p.Pro1398Arg
ENST00000424924.5:c.3167C>G	ENSP00000402944.1:p.Pro1056Arg
ENST00000449833.6:c.3566C>G	ENSP00000399423.3:p.Pro1189Arg
ENST00000601538.5:c.5330C>G	ENSP00000469689.2:p.Pro1777Arg
ENST00000606715.3:n.2082C>G
NM_012309.4:c.5330C>G	NP_036441.2:p.Pro1777Arg
NM_133266.4:c.3566C>G	NP_573573.2:p.Pro1189Arg
NR_110766.1:n.1184C>G
XM_005277930.2:c.5330C>G	XP_005277987.1:p.Pro1777Arg
XM_005277932.2:c.4193C>G	XP_005277989.1:p.Pro1398Arg
XM_006718478.2:c.5300C>G	XP_006718541.1:p.Pro1767Arg
XM_011544854.1:c.5342C>G	XP_011543156.1:p.Pro1781Arg
XM_011544855.1:c.5321C>G	XP_011543157.1:p.Pro1774Arg
XM_011544856.1:c.5315C>G	XP_011543158.1:p.Pro1772Arg
XM_011544857.1:c.5294C>G	XP_011543159.1:p.Pro1765Arg
XM_011544859.1:c.4205C>G	XP_011543161.1:p.Pro1402Arg
XM_005277932.3:c.4193C>G	XP_005277989.1:p.Pro1398Arg
XM_017017387.1:c.5330C>G	XP_016872876.1:p.Pro1777Arg
XM_017017388.1:c.5330C>G	XP_016872877.1:p.Pro1777Arg
XM_017017389.1:c.5303C>G	XP_016872878.1:p.Pro1768Arg
XM_017017390.1:c.3620C>G	XP_016872879.1:p.Pro1207Arg
NM_133266.5:c.3566C>G	NP_573573.2:p.Pro1189Arg
NR_110766.2:n.1185C>G
NM_001379226.1:c.4193C>G	NP_001366155.1:p.Pro1398Arg
NM_012309.5:c.5330C>G MANE Select	NP_036441.2:p.Pro1777Arg