Canonical Allele Identifier: CA381676128

Gene: SHANK2

Linked Data

• MyVariant Identifiers: chr11:g.70319309C>G (hg19) ; chr11:g.70473204C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70473204C>G , CM000673.2:g.70473204C>G	GRCh38
NC_000011.9:g.70319309C>G , CM000673.1:g.70319309C>G	GRCh37
NC_000011.8:g.69996957C>G	NCBI36
NG_042866.1:g.656593G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.3448G>C	ENSP00000345193.7:p.Asp1150His
ENST00000412252.6:c.993G>C	ENSP00000414876.2:n.993G>C
ENST00000601538.6:c.5215G>C MANE Select	ENSP00000469689.2:p.Asp1739His
ENST00000654939.1:c.2724G>C
ENST00000656230.1:c.4078G>C	ENSP00000499561.1:p.Asp1360His
ENST00000659264.1:c.3505G>C	ENSP00000499270.1:p.Asp1169His
ENST00000338508.8:c.3451G>C	ENSP00000345193.6:p.Asp1151His
ENST00000357171.7:c.*219G>C	ENSP00000349694.4:n.*219G>C
ENST00000409161.5:c.3427G>C	ENSP00000386491.1:p.Asp1143His
ENST00000412252.5:c.991G>C
ENST00000423696.6:c.4078G>C	ENSP00000394536.2:p.Asp1360His
ENST00000424924.5:c.3052G>C	ENSP00000402944.1:p.Asp1018His
ENST00000449833.6:c.3451G>C	ENSP00000399423.3:p.Asp1151His
ENST00000601538.5:c.5215G>C	ENSP00000469689.2:p.Asp1739His
ENST00000606715.3:n.1967G>C
NM_012309.4:c.5215G>C	NP_036441.2:p.Asp1739His
NM_133266.4:c.3451G>C	NP_573573.2:p.Asp1151His
NR_110766.1:n.1069G>C
XM_005277930.2:c.5215G>C	XP_005277987.1:p.Asp1739His
XM_005277932.2:c.4078G>C	XP_005277989.1:p.Asp1360His
XM_006718478.2:c.5185G>C	XP_006718541.1:p.Asp1729His
XM_011544854.1:c.5227G>C	XP_011543156.1:p.Asp1743His
XM_011544855.1:c.5206G>C	XP_011543157.1:p.Asp1736His
XM_011544856.1:c.5200G>C	XP_011543158.1:p.Asp1734His
XM_011544857.1:c.5179G>C	XP_011543159.1:p.Asp1727His
XM_011544859.1:c.4090G>C	XP_011543161.1:p.Asp1364His
XM_005277932.3:c.4078G>C	XP_005277989.1:p.Asp1360His
XM_017017387.1:c.5215G>C	XP_016872876.1:p.Asp1739His
XM_017017388.1:c.5215G>C	XP_016872877.1:p.Asp1739His
XM_017017389.1:c.5188G>C	XP_016872878.1:p.Asp1730His
XM_017017390.1:c.3505G>C	XP_016872879.1:p.Asp1169His
NM_133266.5:c.3451G>C	NP_573573.2:p.Asp1151His
NR_110766.2:n.1070G>C
NM_001379226.1:c.4078G>C	NP_001366155.1:p.Asp1360His
NM_012309.5:c.5215G>C MANE Select	NP_036441.2:p.Asp1739His