Canonical Allele Identifier: CA381676814

Gene: SHANK2

Linked Data

• MyVariant Identifiers: chr11:g.70319522T>G (hg19) ; chr11:g.70473417T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70473417T>G , CM000673.2:g.70473417T>G	GRCh38
NC_000011.9:g.70319522T>G , CM000673.1:g.70319522T>G	GRCh37
NC_000011.8:g.69997170T>G	NCBI36
NG_042866.1:g.656380A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.3235A>C	ENSP00000345193.7:p.Ile1079Leu
ENST00000412252.6:c.780A>C	ENSP00000414876.2:n.780A>C
ENST00000601538.6:c.5002A>C MANE Select	ENSP00000469689.2:p.Ile1668Leu
ENST00000654939.1:c.2511A>C
ENST00000656230.1:c.3865A>C	ENSP00000499561.1:p.Ile1289Leu
ENST00000659264.1:c.3292A>C	ENSP00000499270.1:p.Ile1098Leu
ENST00000338508.8:c.3238A>C	ENSP00000345193.6:p.Ile1080Leu
ENST00000357171.7:c.*6A>C	ENSP00000349694.4:n.*6A>C
ENST00000409161.5:c.3214A>C	ENSP00000386491.1:p.Ile1072Leu
ENST00000412252.5:c.778A>C
ENST00000423696.6:c.3865A>C	ENSP00000394536.2:p.Ile1289Leu
ENST00000424924.5:c.2839A>C	ENSP00000402944.1:p.Ile947Leu
ENST00000449833.6:c.3238A>C	ENSP00000399423.3:p.Ile1080Leu
ENST00000601538.5:c.5002A>C	ENSP00000469689.2:p.Ile1668Leu
ENST00000606715.3:n.1754A>C
NM_012309.4:c.5002A>C	NP_036441.2:p.Ile1668Leu
NM_133266.4:c.3238A>C	NP_573573.2:p.Ile1080Leu
NR_110766.1:n.856A>C
XM_005277930.2:c.5002A>C	XP_005277987.1:p.Ile1668Leu
XM_005277932.2:c.3865A>C	XP_005277989.1:p.Ile1289Leu
XM_006718478.2:c.4972A>C	XP_006718541.1:p.Ile1658Leu
XM_011544854.1:c.5014A>C	XP_011543156.1:p.Ile1672Leu
XM_011544855.1:c.4993A>C	XP_011543157.1:p.Ile1665Leu
XM_011544856.1:c.4987A>C	XP_011543158.1:p.Ile1663Leu
XM_011544857.1:c.4966A>C	XP_011543159.1:p.Ile1656Leu
XM_011544859.1:c.3877A>C	XP_011543161.1:p.Ile1293Leu
XM_005277932.3:c.3865A>C	XP_005277989.1:p.Ile1289Leu
XM_017017387.1:c.5002A>C	XP_016872876.1:p.Ile1668Leu
XM_017017388.1:c.5002A>C	XP_016872877.1:p.Ile1668Leu
XM_017017389.1:c.4975A>C	XP_016872878.1:p.Ile1659Leu
XM_017017390.1:c.3292A>C	XP_016872879.1:p.Ile1098Leu
NM_133266.5:c.3238A>C	NP_573573.2:p.Ile1080Leu
NR_110766.2:n.857A>C
NM_001379226.1:c.3865A>C	NP_001366155.1:p.Ile1289Leu
NM_012309.5:c.5002A>C MANE Select	NP_036441.2:p.Ile1668Leu