Canonical Allele Identifier: CA381683760

Gene: SHANK2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70486115G>A , CM000673.2:g.70486115G>A	GRCh38
NC_000011.9:g.70332220G>A , CM000673.1:g.70332220G>A	GRCh37
NC_000011.8:g.70009868G>A	NCBI36
NG_042866.1:g.643682C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338508.9:c.2411C>T	ENSP00000345193.7:p.Pro804Leu
ENST00000412252.6:c.757+4188C>T	ENSP00000414876.2:n.757+4188C>T
ENST00000601538.6:c.4178C>T MANE Select	ENSP00000469689.2:p.Pro1393Leu
ENST00000654939.1:c.1606C>T
ENST00000656230.1:c.3041C>T	ENSP00000499561.1:p.Pro1014Leu
ENST00000659264.1:c.2468C>T	ENSP00000499270.1:p.Pro823Leu
ENST00000338508.8:c.2414C>T	ENSP00000345193.6:p.Pro805Leu
ENST00000357171.7:c.718+4188C>T	ENSP00000349694.4:n.718+4188C>T
ENST00000409161.5:c.2390C>T	ENSP00000386491.1:p.Pro797Leu
ENST00000412252.5:c.755+4188C>T
ENST00000423696.6:c.3041C>T	ENSP00000394536.2:p.Pro1014Leu
ENST00000424924.5:c.2015C>T	ENSP00000402944.1:p.Pro672Leu
ENST00000449833.6:c.2414C>T	ENSP00000399423.3:p.Pro805Leu
ENST00000601538.5:c.4178C>T	ENSP00000469689.2:p.Pro1393Leu
NM_012309.4:c.4178C>T	NP_036441.2:p.Pro1393Leu
NM_133266.4:c.2414C>T	NP_573573.2:p.Pro805Leu
NR_110766.1:n.833+4188C>T
XM_005277930.2:c.4178C>T	XP_005277987.1:p.Pro1393Leu
XM_005277932.2:c.3041C>T	XP_005277989.1:p.Pro1014Leu
XM_006718478.2:c.4148C>T	XP_006718541.1:p.Pro1383Leu
XM_011544854.1:c.4190C>T	XP_011543156.1:p.Pro1397Leu
XM_011544855.1:c.4169C>T	XP_011543157.1:p.Pro1390Leu
XM_011544856.1:c.4163C>T	XP_011543158.1:p.Pro1388Leu
XM_011544857.1:c.4142C>T	XP_011543159.1:p.Pro1381Leu
XM_011544858.1:c.4190C>T	XP_011543160.1:p.Pro1397Leu
XM_011544859.1:c.3053C>T	XP_011543161.1:p.Pro1018Leu
XM_005277932.3:c.3041C>T	XP_005277989.1:p.Pro1014Leu
XM_017017387.1:c.4178C>T	XP_016872876.1:p.Pro1393Leu
XM_017017388.1:c.4178C>T	XP_016872877.1:p.Pro1393Leu
XM_017017389.1:c.4151C>T	XP_016872878.1:p.Pro1384Leu
XM_017017390.1:c.2468C>T	XP_016872879.1:p.Pro823Leu
NM_133266.5:c.2414C>T	NP_573573.2:p.Pro805Leu
NR_110766.2:n.834+4188C>T
NM_001379226.1:c.3041C>T	NP_001366155.1:p.Pro1014Leu
NM_012309.5:c.4178C>T MANE Select	NP_036441.2:p.Pro1393Leu