Canonical Allele Identifier: CA381675912

Gene: SHANK2

Linked Data

• MyVariant Identifiers: chr11:g.70319269A>T (hg19) ; chr11:g.70473164A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70473164A>T , CM000673.2:g.70473164A>T	GRCh38
NC_000011.9:g.70319269A>T , CM000673.1:g.70319269A>T	GRCh37
NC_000011.8:g.69996917A>T	NCBI36
NG_042866.1:g.656633T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.3488T>A	ENSP00000345193.7:p.Leu1163Gln
ENST00000412252.6:c.1033T>A	ENSP00000414876.2:n.1033T>A
ENST00000601538.6:c.5255T>A MANE Select	ENSP00000469689.2:p.Leu1752Gln
ENST00000654939.1:c.2764T>A
ENST00000656230.1:c.4118T>A	ENSP00000499561.1:p.Leu1373Gln
ENST00000659264.1:c.3545T>A	ENSP00000499270.1:p.Leu1182Gln
ENST00000338508.8:c.3491T>A	ENSP00000345193.6:p.Leu1164Gln
ENST00000357171.7:c.*259T>A	ENSP00000349694.4:n.*259T>A
ENST00000409161.5:c.3467T>A	ENSP00000386491.1:p.Leu1156Gln
ENST00000412252.5:c.1031T>A
ENST00000423696.6:c.4118T>A	ENSP00000394536.2:p.Leu1373Gln
ENST00000424924.5:c.3092T>A	ENSP00000402944.1:p.Leu1031Gln
ENST00000449833.6:c.3491T>A	ENSP00000399423.3:p.Leu1164Gln
ENST00000601538.5:c.5255T>A	ENSP00000469689.2:p.Leu1752Gln
ENST00000606715.3:n.2007T>A
NM_012309.4:c.5255T>A	NP_036441.2:p.Leu1752Gln
NM_133266.4:c.3491T>A	NP_573573.2:p.Leu1164Gln
NR_110766.1:n.1109T>A
XM_005277930.2:c.5255T>A	XP_005277987.1:p.Leu1752Gln
XM_005277932.2:c.4118T>A	XP_005277989.1:p.Leu1373Gln
XM_006718478.2:c.5225T>A	XP_006718541.1:p.Leu1742Gln
XM_011544854.1:c.5267T>A	XP_011543156.1:p.Leu1756Gln
XM_011544855.1:c.5246T>A	XP_011543157.1:p.Leu1749Gln
XM_011544856.1:c.5240T>A	XP_011543158.1:p.Leu1747Gln
XM_011544857.1:c.5219T>A	XP_011543159.1:p.Leu1740Gln
XM_011544859.1:c.4130T>A	XP_011543161.1:p.Leu1377Gln
XM_005277932.3:c.4118T>A	XP_005277989.1:p.Leu1373Gln
XM_017017387.1:c.5255T>A	XP_016872876.1:p.Leu1752Gln
XM_017017388.1:c.5255T>A	XP_016872877.1:p.Leu1752Gln
XM_017017389.1:c.5228T>A	XP_016872878.1:p.Leu1743Gln
XM_017017390.1:c.3545T>A	XP_016872879.1:p.Leu1182Gln
NM_133266.5:c.3491T>A	NP_573573.2:p.Leu1164Gln
NR_110766.2:n.1110T>A
NM_001379226.1:c.4118T>A	NP_001366155.1:p.Leu1373Gln
NM_012309.5:c.5255T>A MANE Select	NP_036441.2:p.Leu1752Gln