Canonical Allele Identifier: CA475471288

Gene: SHANK2

Linked Data

• MyVariant Identifiers: chr11:g.70332147A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70486042A>G , CM000673.2:g.70486042A>G	GRCh38
NC_000011.9:g.70332147A>G , CM000673.1:g.70332147A>G	GRCh37
NC_000011.8:g.70009795A>G	NCBI36
NG_042866.1:g.643755T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.2484T>C	ENSP00000345193.7:p.Phe828=
ENST00000412252.6:c.757+4261T>C	ENSP00000414876.2:n.757+4261T>C
ENST00000601538.6:c.4251T>C MANE Select	ENSP00000469689.2:p.Phe1417=
ENST00000654939.1:c.1679T>C
ENST00000656230.1:c.3114T>C	ENSP00000499561.1:p.Phe1038=
ENST00000659264.1:c.2541T>C	ENSP00000499270.1:p.Phe847=
ENST00000338508.8:c.2487T>C	ENSP00000345193.6:p.Phe829=
ENST00000357171.7:c.718+4261T>C	ENSP00000349694.4:n.718+4261T>C
ENST00000409161.5:c.2463T>C	ENSP00000386491.1:p.Phe821=
ENST00000412252.5:c.755+4261T>C
ENST00000423696.6:c.3114T>C	ENSP00000394536.2:p.Phe1038=
ENST00000424924.5:c.2088T>C	ENSP00000402944.1:p.Phe696=
ENST00000449833.6:c.2487T>C	ENSP00000399423.3:p.Phe829=
ENST00000601538.5:c.4251T>C	ENSP00000469689.2:p.Phe1417=
NM_012309.4:c.4251T>C	NP_036441.2:p.Phe1417=
NM_133266.4:c.2487T>C	NP_573573.2:p.Phe829=
NR_110766.1:n.833+4261T>C
XM_005277930.2:c.4251T>C	XP_005277987.1:p.Phe1417=
XM_005277932.2:c.3114T>C	XP_005277989.1:p.Phe1038=
XM_006718478.2:c.4221T>C	XP_006718541.1:p.Phe1407=
XM_011544854.1:c.4263T>C	XP_011543156.1:p.Phe1421=
XM_011544855.1:c.4242T>C	XP_011543157.1:p.Phe1414=
XM_011544856.1:c.4236T>C	XP_011543158.1:p.Phe1412=
XM_011544857.1:c.4215T>C	XP_011543159.1:p.Phe1405=
XM_011544858.1:c.4263T>C	XP_011543160.1:p.Phe1421=
XM_011544859.1:c.3126T>C	XP_011543161.1:p.Phe1042=
XM_005277932.3:c.3114T>C	XP_005277989.1:p.Phe1038=
XM_017017387.1:c.4251T>C	XP_016872876.1:p.Phe1417=
XM_017017388.1:c.4251T>C	XP_016872877.1:p.Phe1417=
XM_017017389.1:c.4224T>C	XP_016872878.1:p.Phe1408=
XM_017017390.1:c.2541T>C	XP_016872879.1:p.Phe847=
NM_133266.5:c.2487T>C	NP_573573.2:p.Phe829=
NR_110766.2:n.834+4261T>C
NM_001379226.1:c.3114T>C	NP_001366155.1:p.Phe1038=
NM_012309.5:c.4251T>C MANE Select	NP_036441.2:p.Phe1417=