Canonical Allele Identifier: CA475471110

Gene: SHANK2

Linked Data

• MyVariant Identifiers: chr11:g.70319226G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70473121G>T , CM000673.2:g.70473121G>T	GRCh38
NC_000011.9:g.70319226G>T , CM000673.1:g.70319226G>T	GRCh37
NC_000011.8:g.69996874G>T	NCBI36
NG_042866.1:g.656676C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.3531C>A	ENSP00000345193.7:p.Pro1177=
ENST00000412252.6:c.1076C>A	ENSP00000414876.2:n.1076C>A
ENST00000601538.6:c.5298C>A MANE Select	ENSP00000469689.2:p.Pro1766=
ENST00000654939.1:c.2807C>A
ENST00000656230.1:c.4161C>A	ENSP00000499561.1:p.Pro1387=
ENST00000659264.1:c.3588C>A	ENSP00000499270.1:p.Pro1196=
ENST00000338508.8:c.3534C>A	ENSP00000345193.6:p.Pro1178=
ENST00000357171.7:c.*302C>A	ENSP00000349694.4:n.*302C>A
ENST00000409161.5:c.3510C>A	ENSP00000386491.1:p.Pro1170=
ENST00000412252.5:c.1074C>A
ENST00000423696.6:c.4161C>A	ENSP00000394536.2:p.Pro1387=
ENST00000424924.5:c.3135C>A	ENSP00000402944.1:p.Pro1045=
ENST00000449833.6:c.3534C>A	ENSP00000399423.3:p.Pro1178=
ENST00000601538.5:c.5298C>A	ENSP00000469689.2:p.Pro1766=
ENST00000606715.3:n.2050C>A
NM_012309.4:c.5298C>A	NP_036441.2:p.Pro1766=
NM_133266.4:c.3534C>A	NP_573573.2:p.Pro1178=
NR_110766.1:n.1152C>A
XM_005277930.2:c.5298C>A	XP_005277987.1:p.Pro1766=
XM_005277932.2:c.4161C>A	XP_005277989.1:p.Pro1387=
XM_006718478.2:c.5268C>A	XP_006718541.1:p.Pro1756=
XM_011544854.1:c.5310C>A	XP_011543156.1:p.Pro1770=
XM_011544855.1:c.5289C>A	XP_011543157.1:p.Pro1763=
XM_011544856.1:c.5283C>A	XP_011543158.1:p.Pro1761=
XM_011544857.1:c.5262C>A	XP_011543159.1:p.Pro1754=
XM_011544859.1:c.4173C>A	XP_011543161.1:p.Pro1391=
XM_005277932.3:c.4161C>A	XP_005277989.1:p.Pro1387=
XM_017017387.1:c.5298C>A	XP_016872876.1:p.Pro1766=
XM_017017388.1:c.5298C>A	XP_016872877.1:p.Pro1766=
XM_017017389.1:c.5271C>A	XP_016872878.1:p.Pro1757=
XM_017017390.1:c.3588C>A	XP_016872879.1:p.Pro1196=
NM_133266.5:c.3534C>A	NP_573573.2:p.Pro1178=
NR_110766.2:n.1153C>A
NM_001379226.1:c.4161C>A	NP_001366155.1:p.Pro1387=
NM_012309.5:c.5298C>A MANE Select	NP_036441.2:p.Pro1766=