Canonical Allele Identifier: CA381683017

Gene: SHANK2

Linked Data

• MyVariant Identifiers: chr11:g.70332115G>A (hg19) ; chr11:g.70486010G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70486010G>A , CM000673.2:g.70486010G>A	GRCh38
NC_000011.9:g.70332115G>A , CM000673.1:g.70332115G>A	GRCh37
NC_000011.8:g.70009763G>A	NCBI36
NG_042866.1:g.643787C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000338508.9:c.2516C>T	ENSP00000345193.7:p.Ala839Val
ENST00000412252.6:c.757+4293C>T	ENSP00000414876.2:n.757+4293C>T
ENST00000601538.6:c.4283C>T MANE Select	ENSP00000469689.2:p.Ala1428Val
ENST00000654939.1:c.1711C>T
ENST00000656230.1:c.3146C>T	ENSP00000499561.1:p.Ala1049Val
ENST00000659264.1:c.2573C>T	ENSP00000499270.1:p.Ala858Val
ENST00000338508.8:c.2519C>T	ENSP00000345193.6:p.Ala840Val
ENST00000357171.7:c.718+4293C>T	ENSP00000349694.4:n.718+4293C>T
ENST00000409161.5:c.2495C>T	ENSP00000386491.1:p.Ala832Val
ENST00000412252.5:c.755+4293C>T
ENST00000423696.6:c.3146C>T	ENSP00000394536.2:p.Ala1049Val
ENST00000424924.5:c.2120C>T	ENSP00000402944.1:p.Ala707Val
ENST00000449833.6:c.2519C>T	ENSP00000399423.3:p.Ala840Val
ENST00000601538.5:c.4283C>T	ENSP00000469689.2:p.Ala1428Val
NM_012309.4:c.4283C>T	NP_036441.2:p.Ala1428Val
NM_133266.4:c.2519C>T	NP_573573.2:p.Ala840Val
NR_110766.1:n.833+4293C>T
XM_005277930.2:c.4283C>T	XP_005277987.1:p.Ala1428Val
XM_005277932.2:c.3146C>T	XP_005277989.1:p.Ala1049Val
XM_006718478.2:c.4253C>T	XP_006718541.1:p.Ala1418Val
XM_011544854.1:c.4295C>T	XP_011543156.1:p.Ala1432Val
XM_011544855.1:c.4274C>T	XP_011543157.1:p.Ala1425Val
XM_011544856.1:c.4268C>T	XP_011543158.1:p.Ala1423Val
XM_011544857.1:c.4247C>T	XP_011543159.1:p.Ala1416Val
XM_011544858.1:c.4295C>T	XP_011543160.1:p.Ala1432Val
XM_011544859.1:c.3158C>T	XP_011543161.1:p.Ala1053Val
XM_005277932.3:c.3146C>T	XP_005277989.1:p.Ala1049Val
XM_017017387.1:c.4283C>T	XP_016872876.1:p.Ala1428Val
XM_017017388.1:c.4283C>T	XP_016872877.1:p.Ala1428Val
XM_017017389.1:c.4256C>T	XP_016872878.1:p.Ala1419Val
XM_017017390.1:c.2573C>T	XP_016872879.1:p.Ala858Val
NM_133266.5:c.2519C>T	NP_573573.2:p.Ala840Val
NR_110766.2:n.834+4293C>T
NM_001379226.1:c.3146C>T	NP_001366155.1:p.Ala1049Val
NM_012309.5:c.4283C>T MANE Select	NP_036441.2:p.Ala1428Val