Canonical Allele Identifier: CA381675842

Gene: SHANK2

Linked Data

• MyVariant Identifiers: chr11:g.70319256G>C (hg19) ; chr11:g.70473151G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70473151G>C , CM000673.2:g.70473151G>C	GRCh38
NC_000011.9:g.70319256G>C , CM000673.1:g.70319256G>C	GRCh37
NC_000011.8:g.69996904G>C	NCBI36
NG_042866.1:g.656646C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.3501C>G	ENSP00000345193.7:p.Asn1167Lys
ENST00000412252.6:c.1046C>G	ENSP00000414876.2:n.1046C>G
ENST00000601538.6:c.5268C>G MANE Select	ENSP00000469689.2:p.Asn1756Lys
ENST00000654939.1:c.2777C>G
ENST00000656230.1:c.4131C>G	ENSP00000499561.1:p.Asn1377Lys
ENST00000659264.1:c.3558C>G	ENSP00000499270.1:p.Asn1186Lys
ENST00000338508.8:c.3504C>G	ENSP00000345193.6:p.Asn1168Lys
ENST00000357171.7:c.*272C>G	ENSP00000349694.4:n.*272C>G
ENST00000409161.5:c.3480C>G	ENSP00000386491.1:p.Asn1160Lys
ENST00000412252.5:c.1044C>G
ENST00000423696.6:c.4131C>G	ENSP00000394536.2:p.Asn1377Lys
ENST00000424924.5:c.3105C>G	ENSP00000402944.1:p.Asn1035Lys
ENST00000449833.6:c.3504C>G	ENSP00000399423.3:p.Asn1168Lys
ENST00000601538.5:c.5268C>G	ENSP00000469689.2:p.Asn1756Lys
ENST00000606715.3:n.2020C>G
NM_012309.4:c.5268C>G	NP_036441.2:p.Asn1756Lys
NM_133266.4:c.3504C>G	NP_573573.2:p.Asn1168Lys
NR_110766.1:n.1122C>G
XM_005277930.2:c.5268C>G	XP_005277987.1:p.Asn1756Lys
XM_005277932.2:c.4131C>G	XP_005277989.1:p.Asn1377Lys
XM_006718478.2:c.5238C>G	XP_006718541.1:p.Asn1746Lys
XM_011544854.1:c.5280C>G	XP_011543156.1:p.Asn1760Lys
XM_011544855.1:c.5259C>G	XP_011543157.1:p.Asn1753Lys
XM_011544856.1:c.5253C>G	XP_011543158.1:p.Asn1751Lys
XM_011544857.1:c.5232C>G	XP_011543159.1:p.Asn1744Lys
XM_011544859.1:c.4143C>G	XP_011543161.1:p.Asn1381Lys
XM_005277932.3:c.4131C>G	XP_005277989.1:p.Asn1377Lys
XM_017017387.1:c.5268C>G	XP_016872876.1:p.Asn1756Lys
XM_017017388.1:c.5268C>G	XP_016872877.1:p.Asn1756Lys
XM_017017389.1:c.5241C>G	XP_016872878.1:p.Asn1747Lys
XM_017017390.1:c.3558C>G	XP_016872879.1:p.Asn1186Lys
NM_133266.5:c.3504C>G	NP_573573.2:p.Asn1168Lys
NR_110766.2:n.1123C>G
NM_001379226.1:c.4131C>G	NP_001366155.1:p.Asn1377Lys
NM_012309.5:c.5268C>G MANE Select	NP_036441.2:p.Asn1756Lys