Canonical Allele Identifier: CA10445067

Gene: NLGN3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71155351G>A , CM000685.2:g.71155351G>A	GRCh38
NC_000023.10:g.70375201G>A , CM000685.1:g.70375201G>A	GRCh37
NC_000023.9:g.70291926G>A	NCBI36
NG_015874.1:g.15521G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395855.7:c.595G>A	ENSP00000379196.3:p.Val199Ile
ENST00000476589.2:n.894G>A
ENST00000536169.6:c.595G>A	ENSP00000445298.1:p.Val199Ile
ENST00000685718.1:c.655G>A	ENSP00000510514.1:p.Val219Ile
ENST00000687220.1:c.364G>A	ENSP00000509531.1:p.Val122Ile
ENST00000687470.1:c.715G>A	ENSP00000508881.1:p.Val239Ile
ENST00000687568.1:c.595G>A	ENSP00000509635.1:p.Val199Ile
ENST00000688566.1:c.364G>A	ENSP00000509202.1:p.Val122Ile
ENST00000688950.1:n.1698G>A
ENST00000689857.1:c.457+7145G>A	ENSP00000510719.1:n.457+7145G>A
ENST00000689968.1:c.655G>A	ENSP00000510150.1:p.Val219Ile
ENST00000690133.1:c.304G>A	ENSP00000508912.1:p.Val102Ile
ENST00000690293.1:c.*255G>A	ENSP00000509154.1:n.*255G>A
ENST00000691045.1:n.602G>A
ENST00000692338.1:c.304G>A	ENSP00000508700.1:p.Val102Ile
ENST00000692468.1:n.219G>A
ENST00000692905.1:c.655G>A	ENSP00000510435.1:p.Val219Ile
ENST00000358741.4:c.715G>A MANE Select	ENSP00000351591.4:p.Val239Ile
ENST00000358741.3:c.715G>A	ENSP00000351591.3:p.Val239Ile
ENST00000374051.7:c.655G>A	ENSP00000363163.3:p.Val219Ile
ENST00000395855.6:c.595G>A	ENSP00000379196.2:p.Val199Ile
ENST00000476589.1:n.219G>A
ENST00000536169.5:c.595G>A	ENSP00000445298.1:p.Val199Ile
ENST00000612180.4:c.304G>A	ENSP00000479877.1:p.Val102Ile
NM_001166660.1:c.595G>A	NP_001160132.1:p.Val199Ile
NM_018977.3:c.655G>A	NP_061850.2:p.Val219Ile
NM_181303.1:c.715G>A	NP_851820.1:p.Val239Ile
XM_005262279.2:c.715G>A	XP_005262336.1:p.Val239Ile
XM_006724662.2:c.568G>A	XP_006724725.2:p.Val190Ile
XM_006724663.2:c.364G>A	XP_006724726.1:p.Val122Ile
XM_011530974.1:c.364G>A	XP_011529276.1:p.Val122Ile
XM_011530975.1:c.304G>A	XP_011529277.1:p.Val102Ile
NM_001321276.1:c.304G>A	NP_001308205.1:p.Val102Ile
XM_006724662.4:c.568G>A	XP_006724725.2:p.Val190Ile
XM_006724663.4:c.364G>A	XP_006724726.1:p.Val122Ile
XM_011530974.3:c.364G>A	XP_011529276.1:p.Val122Ile
XM_017029597.2:c.715G>A	XP_016885086.1:p.Val239Ile
NM_001321276.2:c.304G>A	NP_001308205.1:p.Val102Ile
NM_018977.4:c.655G>A	NP_061850.2:p.Val219Ile
NM_181303.2:c.715G>A MANE Select	NP_851820.1:p.Val239Ile
NM_001166660.2:c.595G>A	NP_001160132.1:p.Val199Ile