Canonical Allele Identifier: CA381676116

Gene: SHANK2

Linked Data

• MyVariant Identifiers: chr11:g.70319308T>A (hg19) ; chr11:g.70473203T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70473203T>A , CM000673.2:g.70473203T>A	GRCh38
NC_000011.9:g.70319308T>A , CM000673.1:g.70319308T>A	GRCh37
NC_000011.8:g.69996956T>A	NCBI36
NG_042866.1:g.656594A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.3449A>T	ENSP00000345193.7:p.Asp1150Val
ENST00000412252.6:c.994A>T	ENSP00000414876.2:n.994A>T
ENST00000601538.6:c.5216A>T MANE Select	ENSP00000469689.2:p.Asp1739Val
ENST00000654939.1:c.2725A>T
ENST00000656230.1:c.4079A>T	ENSP00000499561.1:p.Asp1360Val
ENST00000659264.1:c.3506A>T	ENSP00000499270.1:p.Asp1169Val
ENST00000338508.8:c.3452A>T	ENSP00000345193.6:p.Asp1151Val
ENST00000357171.7:c.*220A>T	ENSP00000349694.4:n.*220A>T
ENST00000409161.5:c.3428A>T	ENSP00000386491.1:p.Asp1143Val
ENST00000412252.5:c.992A>T
ENST00000423696.6:c.4079A>T	ENSP00000394536.2:p.Asp1360Val
ENST00000424924.5:c.3053A>T	ENSP00000402944.1:p.Asp1018Val
ENST00000449833.6:c.3452A>T	ENSP00000399423.3:p.Asp1151Val
ENST00000601538.5:c.5216A>T	ENSP00000469689.2:p.Asp1739Val
ENST00000606715.3:n.1968A>T
NM_012309.4:c.5216A>T	NP_036441.2:p.Asp1739Val
NM_133266.4:c.3452A>T	NP_573573.2:p.Asp1151Val
NR_110766.1:n.1070A>T
XM_005277930.2:c.5216A>T	XP_005277987.1:p.Asp1739Val
XM_005277932.2:c.4079A>T	XP_005277989.1:p.Asp1360Val
XM_006718478.2:c.5186A>T	XP_006718541.1:p.Asp1729Val
XM_011544854.1:c.5228A>T	XP_011543156.1:p.Asp1743Val
XM_011544855.1:c.5207A>T	XP_011543157.1:p.Asp1736Val
XM_011544856.1:c.5201A>T	XP_011543158.1:p.Asp1734Val
XM_011544857.1:c.5180A>T	XP_011543159.1:p.Asp1727Val
XM_011544859.1:c.4091A>T	XP_011543161.1:p.Asp1364Val
XM_005277932.3:c.4079A>T	XP_005277989.1:p.Asp1360Val
XM_017017387.1:c.5216A>T	XP_016872876.1:p.Asp1739Val
XM_017017388.1:c.5216A>T	XP_016872877.1:p.Asp1739Val
XM_017017389.1:c.5189A>T	XP_016872878.1:p.Asp1730Val
XM_017017390.1:c.3506A>T	XP_016872879.1:p.Asp1169Val
NM_133266.5:c.3452A>T	NP_573573.2:p.Asp1151Val
NR_110766.2:n.1071A>T
NM_001379226.1:c.4079A>T	NP_001366155.1:p.Asp1360Val
NM_012309.5:c.5216A>T MANE Select	NP_036441.2:p.Asp1739Val