Canonical Allele Identifier: CA381676221

Gene: SHANK2

Linked Data

• MyVariant Identifiers: chr11:g.70319338G>T (hg19) ; chr11:g.70473233G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70473233G>T , CM000673.2:g.70473233G>T	GRCh38
NC_000011.9:g.70319338G>T , CM000673.1:g.70319338G>T	GRCh37
NC_000011.8:g.69996986G>T	NCBI36
NG_042866.1:g.656564C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.3419C>A	ENSP00000345193.7:p.Ala1140Asp
ENST00000412252.6:c.964C>A	ENSP00000414876.2:n.964C>A
ENST00000601538.6:c.5186C>A MANE Select	ENSP00000469689.2:p.Ala1729Asp
ENST00000654939.1:c.2695C>A
ENST00000656230.1:c.4049C>A	ENSP00000499561.1:p.Ala1350Asp
ENST00000659264.1:c.3476C>A	ENSP00000499270.1:p.Ala1159Asp
ENST00000338508.8:c.3422C>A	ENSP00000345193.6:p.Ala1141Asp
ENST00000357171.7:c.*190C>A	ENSP00000349694.4:n.*190C>A
ENST00000409161.5:c.3398C>A	ENSP00000386491.1:p.Ala1133Asp
ENST00000412252.5:c.962C>A
ENST00000423696.6:c.4049C>A	ENSP00000394536.2:p.Ala1350Asp
ENST00000424924.5:c.3023C>A	ENSP00000402944.1:p.Ala1008Asp
ENST00000449833.6:c.3422C>A	ENSP00000399423.3:p.Ala1141Asp
ENST00000601538.5:c.5186C>A	ENSP00000469689.2:p.Ala1729Asp
ENST00000606715.3:n.1938C>A
NM_012309.4:c.5186C>A	NP_036441.2:p.Ala1729Asp
NM_133266.4:c.3422C>A	NP_573573.2:p.Ala1141Asp
NR_110766.1:n.1040C>A
XM_005277930.2:c.5186C>A	XP_005277987.1:p.Ala1729Asp
XM_005277932.2:c.4049C>A	XP_005277989.1:p.Ala1350Asp
XM_006718478.2:c.5156C>A	XP_006718541.1:p.Ala1719Asp
XM_011544854.1:c.5198C>A	XP_011543156.1:p.Ala1733Asp
XM_011544855.1:c.5177C>A	XP_011543157.1:p.Ala1726Asp
XM_011544856.1:c.5171C>A	XP_011543158.1:p.Ala1724Asp
XM_011544857.1:c.5150C>A	XP_011543159.1:p.Ala1717Asp
XM_011544859.1:c.4061C>A	XP_011543161.1:p.Ala1354Asp
XM_005277932.3:c.4049C>A	XP_005277989.1:p.Ala1350Asp
XM_017017387.1:c.5186C>A	XP_016872876.1:p.Ala1729Asp
XM_017017388.1:c.5186C>A	XP_016872877.1:p.Ala1729Asp
XM_017017389.1:c.5159C>A	XP_016872878.1:p.Ala1720Asp
XM_017017390.1:c.3476C>A	XP_016872879.1:p.Ala1159Asp
NM_133266.5:c.3422C>A	NP_573573.2:p.Ala1141Asp
NR_110766.2:n.1041C>A
NM_001379226.1:c.4049C>A	NP_001366155.1:p.Ala1350Asp
NM_012309.5:c.5186C>A MANE Select	NP_036441.2:p.Ala1729Asp