Canonical Allele Identifier: CA381675472

Gene: SHANK2

Linked Data

• MyVariant Identifiers: chr11:g.70319201T>A (hg19) ; chr11:g.70473096T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70473096T>A , CM000673.2:g.70473096T>A	GRCh38
NC_000011.9:g.70319201T>A , CM000673.1:g.70319201T>A	GRCh37
NC_000011.8:g.69996849T>A	NCBI36
NG_042866.1:g.656701A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.3556A>T	ENSP00000345193.7:p.Asn1186Tyr
ENST00000412252.6:c.1101A>T	ENSP00000414876.2:n.1101A>T
ENST00000601538.6:c.5323A>T MANE Select	ENSP00000469689.2:p.Asn1775Tyr
ENST00000654939.1:c.2832A>T
ENST00000656230.1:c.4186A>T	ENSP00000499561.1:p.Asn1396Tyr
ENST00000659264.1:c.3613A>T	ENSP00000499270.1:p.Asn1205Tyr
ENST00000338508.8:c.3559A>T	ENSP00000345193.6:p.Asn1187Tyr
ENST00000357171.7:c.*327A>T	ENSP00000349694.4:n.*327A>T
ENST00000409161.5:c.3535A>T	ENSP00000386491.1:p.Asn1179Tyr
ENST00000412252.5:c.1099A>T
ENST00000423696.6:c.4186A>T	ENSP00000394536.2:p.Asn1396Tyr
ENST00000424924.5:c.3160A>T	ENSP00000402944.1:p.Asn1054Tyr
ENST00000449833.6:c.3559A>T	ENSP00000399423.3:p.Asn1187Tyr
ENST00000601538.5:c.5323A>T	ENSP00000469689.2:p.Asn1775Tyr
ENST00000606715.3:n.2075A>T
NM_012309.4:c.5323A>T	NP_036441.2:p.Asn1775Tyr
NM_133266.4:c.3559A>T	NP_573573.2:p.Asn1187Tyr
NR_110766.1:n.1177A>T
XM_005277930.2:c.5323A>T	XP_005277987.1:p.Asn1775Tyr
XM_005277932.2:c.4186A>T	XP_005277989.1:p.Asn1396Tyr
XM_006718478.2:c.5293A>T	XP_006718541.1:p.Asn1765Tyr
XM_011544854.1:c.5335A>T	XP_011543156.1:p.Asn1779Tyr
XM_011544855.1:c.5314A>T	XP_011543157.1:p.Asn1772Tyr
XM_011544856.1:c.5308A>T	XP_011543158.1:p.Asn1770Tyr
XM_011544857.1:c.5287A>T	XP_011543159.1:p.Asn1763Tyr
XM_011544859.1:c.4198A>T	XP_011543161.1:p.Asn1400Tyr
XM_005277932.3:c.4186A>T	XP_005277989.1:p.Asn1396Tyr
XM_017017387.1:c.5323A>T	XP_016872876.1:p.Asn1775Tyr
XM_017017388.1:c.5323A>T	XP_016872877.1:p.Asn1775Tyr
XM_017017389.1:c.5296A>T	XP_016872878.1:p.Asn1766Tyr
XM_017017390.1:c.3613A>T	XP_016872879.1:p.Asn1205Tyr
NM_133266.5:c.3559A>T	NP_573573.2:p.Asn1187Tyr
NR_110766.2:n.1178A>T
NM_001379226.1:c.4186A>T	NP_001366155.1:p.Asn1396Tyr
NM_012309.5:c.5323A>T MANE Select	NP_036441.2:p.Asn1775Tyr