Canonical Allele Identifier: CA877814391

Gene: NLGN3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71148209G>A , CM000685.2:g.71148209G>A	GRCh38
NC_000023.10:g.70368059G>A , CM000685.1:g.70368059G>A	GRCh37
NC_000023.9:g.70284784G>A	NCBI36
NG_015874.1:g.8379G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_181303.2:c.457+3G>A MANE Select	NP_851820.1:n.457+3G>A
ENST00000358741.4:c.457+3G>A MANE Select	ENSP00000351591.4:n.457+3G>A
NM_001166660.1:c.457+3G>A	NP_001160132.1:n.457+3G>A
NM_001166660.2:c.457+3G>A	NP_001160132.1:n.457+3G>A
NM_001321276.1:c.106+3G>A	NP_001308205.1:n.106+3G>A
NM_001321276.2:c.106+3G>A	NP_001308205.1:n.106+3G>A
NM_018977.3:c.457+3G>A	NP_061850.2:n.457+3G>A
NM_018977.4:c.457+3G>A	NP_061850.2:n.457+3G>A
NM_181303.1:c.457+3G>A	NP_851820.1:n.457+3G>A
ENST00000358741.3:c.457+3G>A	ENSP00000351591.3:n.457+3G>A
ENST00000374051.7:c.457+3G>A	ENSP00000363163.3:n.457+3G>A
ENST00000395855.6:c.457+3G>A	ENSP00000379196.2:n.457+3G>A
ENST00000395855.7:c.457+3G>A	ENSP00000379196.3:n.457+3G>A
ENST00000476589.2:n.696+3G>A
ENST00000536169.5:c.457+3G>A	ENSP00000445298.1:n.457+3G>A
ENST00000536169.6:c.457+3G>A	ENSP00000445298.1:n.457+3G>A
ENST00000612180.4:c.106+3G>A	ENSP00000479877.1:n.106+3G>A
ENST00000685718.1:c.457+3G>A	ENSP00000510514.1:n.457+3G>A
ENST00000687220.1:c.106+3G>A	ENSP00000509531.1:n.106+3G>A
ENST00000687470.1:c.457+3G>A	ENSP00000508881.1:n.457+3G>A
ENST00000687568.1:c.457+3G>A	ENSP00000509635.1:n.457+3G>A
ENST00000688566.1:c.106+3G>A	ENSP00000509202.1:n.106+3G>A
ENST00000688950.1:n.804G>A
ENST00000689857.1:c.457+3G>A	ENSP00000510719.1:n.457+3G>A
ENST00000689968.1:c.457+3G>A	ENSP00000510150.1:n.457+3G>A
ENST00000690133.1:c.106+3G>A	ENSP00000508912.1:n.106+3G>A
ENST00000690293.1:c.106+3G>A	ENSP00000509154.1:n.106+3G>A
ENST00000691045.1:n.464+3G>A
ENST00000692338.1:c.106+3G>A	ENSP00000508700.1:n.106+3G>A
ENST00000692800.1:n.804G>A
ENST00000692905.1:c.457+3G>A	ENSP00000510435.1:n.457+3G>A
XM_005262279.2:c.457+3G>A	XP_005262336.1:n.457+3G>A
XM_006724662.2:c.310+3G>A	XP_006724725.2:n.310+3G>A
XM_006724662.4:c.310+3G>A	XP_006724725.2:n.310+3G>A
XM_006724663.2:c.106+3G>A	XP_006724726.1:n.106+3G>A
XM_006724663.4:c.106+3G>A	XP_006724726.1:n.106+3G>A
XM_011530974.1:c.106+3G>A	XP_011529276.1:n.106+3G>A
XM_011530974.3:c.106+3G>A	XP_011529276.1:n.106+3G>A
XM_011530975.1:c.106+3G>A	XP_011529277.1:n.106+3G>A
XM_017029597.2:c.457+3G>A	XP_016885086.1:n.457+3G>A
XR_938431.1:n.136+2074C>T