Canonical Allele Identifier: CA1981067927

Gene: SHANK2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70473146G= , CM000673.2:g.70473146G=	GRCh38
NC_000011.9:g.70319251G= , CM000673.1:g.70319251G=	GRCh37
NC_000011.8:g.69996899G=	NCBI36
NG_042866.1:g.656651C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.3506C=	ENSP00000345193.7:p.Ala1169=
ENST00000412252.6:c.1051C=	ENSP00000414876.2:n.1051C=
ENST00000601538.6:c.5273C= MANE Select	ENSP00000469689.2:p.Ala1758=
ENST00000654939.1:c.2782C=
ENST00000656230.1:c.4136C=	ENSP00000499561.1:p.Ala1379=
ENST00000659264.1:c.3563C=	ENSP00000499270.1:p.Ala1188=
ENST00000338508.8:c.3509C=	ENSP00000345193.6:p.Ala1170=
ENST00000357171.7:c.*277C=	ENSP00000349694.4:n.*277C=
ENST00000409161.5:c.3485C=	ENSP00000386491.1:p.Ala1162=
ENST00000412252.5:c.1049C=
ENST00000423696.6:c.4136C=	ENSP00000394536.2:p.Ala1379=
ENST00000424924.5:c.3110C=	ENSP00000402944.1:p.Ala1037=
ENST00000449833.6:c.3509C=	ENSP00000399423.3:p.Ala1170=
ENST00000601538.5:c.5273C=	ENSP00000469689.2:p.Ala1758=
ENST00000606715.3:n.2025C=
NM_012309.4:c.5273C=	NP_036441.2:p.Ala1758=
NM_133266.4:c.3509C=	NP_573573.2:p.Ala1170=
NR_110766.1:n.1127C=
XM_005277930.2:c.5273C=	XP_005277987.1:p.Ala1758=
XM_005277932.2:c.4136C=	XP_005277989.1:p.Ala1379=
XM_006718478.2:c.5243C=	XP_006718541.1:p.Ala1748=
XM_011544854.1:c.5285C=	XP_011543156.1:p.Ala1762=
XM_011544855.1:c.5264C=	XP_011543157.1:p.Ala1755=
XM_011544856.1:c.5258C=	XP_011543158.1:p.Ala1753=
XM_011544857.1:c.5237C=	XP_011543159.1:p.Ala1746=
XM_011544859.1:c.4148C=	XP_011543161.1:p.Ala1383=
XM_005277932.3:c.4136C=	XP_005277989.1:p.Ala1379=
XM_017017387.1:c.5273C=	XP_016872876.1:p.Ala1758=
XM_017017388.1:c.5273C=	XP_016872877.1:p.Ala1758=
XM_017017389.1:c.5246C=	XP_016872878.1:p.Ala1749=
XM_017017390.1:c.3563C=	XP_016872879.1:p.Ala1188=
NM_133266.5:c.3509C=	NP_573573.2:p.Ala1170=
NR_110766.2:n.1128C=
NM_001379226.1:c.4136C=	NP_001366155.1:p.Ala1379=
NM_012309.5:c.5273C= MANE Select	NP_036441.2:p.Ala1758=