Canonical Allele Identifier: CA1981067937

Gene: SHANK2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70473178G= , CM000673.2:g.70473178G=	GRCh38
NC_000011.9:g.70319283G= , CM000673.1:g.70319283G=	GRCh37
NC_000011.8:g.69996931G=	NCBI36
NG_042866.1:g.656619C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.3474C=	ENSP00000345193.7:p.Pro1158=
ENST00000412252.6:c.1019C=	ENSP00000414876.2:n.1019C=
ENST00000601538.6:c.5241C= MANE Select	ENSP00000469689.2:p.Pro1747=
ENST00000654939.1:c.2750C=
ENST00000656230.1:c.4104C=	ENSP00000499561.1:p.Pro1368=
ENST00000659264.1:c.3531C=	ENSP00000499270.1:p.Pro1177=
ENST00000338508.8:c.3477C=	ENSP00000345193.6:p.Pro1159=
ENST00000357171.7:c.*245C=	ENSP00000349694.4:n.*245C=
ENST00000409161.5:c.3453C=	ENSP00000386491.1:p.Pro1151=
ENST00000412252.5:c.1017C=
ENST00000423696.6:c.4104C=	ENSP00000394536.2:p.Pro1368=
ENST00000424924.5:c.3078C=	ENSP00000402944.1:p.Pro1026=
ENST00000449833.6:c.3477C=	ENSP00000399423.3:p.Pro1159=
ENST00000601538.5:c.5241C=	ENSP00000469689.2:p.Pro1747=
ENST00000606715.3:n.1993C=
NM_012309.4:c.5241C=	NP_036441.2:p.Pro1747=
NM_133266.4:c.3477C=	NP_573573.2:p.Pro1159=
NR_110766.1:n.1095C=
XM_005277930.2:c.5241C=	XP_005277987.1:p.Pro1747=
XM_005277932.2:c.4104C=	XP_005277989.1:p.Pro1368=
XM_006718478.2:c.5211C=	XP_006718541.1:p.Pro1737=
XM_011544854.1:c.5253C=	XP_011543156.1:p.Pro1751=
XM_011544855.1:c.5232C=	XP_011543157.1:p.Pro1744=
XM_011544856.1:c.5226C=	XP_011543158.1:p.Pro1742=
XM_011544857.1:c.5205C=	XP_011543159.1:p.Pro1735=
XM_011544859.1:c.4116C=	XP_011543161.1:p.Pro1372=
XM_005277932.3:c.4104C=	XP_005277989.1:p.Pro1368=
XM_017017387.1:c.5241C=	XP_016872876.1:p.Pro1747=
XM_017017388.1:c.5241C=	XP_016872877.1:p.Pro1747=
XM_017017389.1:c.5214C=	XP_016872878.1:p.Pro1738=
XM_017017390.1:c.3531C=	XP_016872879.1:p.Pro1177=
NM_133266.5:c.3477C=	NP_573573.2:p.Pro1159=
NR_110766.2:n.1096C=
NM_001379226.1:c.4104C=	NP_001366155.1:p.Pro1368=
NM_012309.5:c.5241C= MANE Select	NP_036441.2:p.Pro1747=