Canonical Allele Identifier: CA516731512

Gene: NLGN3

Linked Data

• MyVariant Identifiers: chrX:g.70389161C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71169311C>A , CM000685.2:g.71169311C>A	GRCh38
NC_000023.10:g.70389161C>A , CM000685.1:g.70389161C>A	GRCh37
NC_000023.9:g.70305886C>A	NCBI36
NG_015874.1:g.29481C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000476589.2:n.1940C>A
ENST00000536169.6:c.1641C>A	ENSP00000445298.1:p.Arg547=
ENST00000685718.1:c.*1108C>A	ENSP00000510514.1:n.*1108C>A
ENST00000685950.1:n.3436C>A
ENST00000687220.1:c.1410C>A	ENSP00000509531.1:p.Arg470=
ENST00000687470.1:c.1761C>A	ENSP00000508881.1:p.Arg587=
ENST00000687568.1:c.851C>A	ENSP00000509635.1:p.Ala284Asp
ENST00000688566.1:c.1410C>A	ENSP00000509202.1:p.Arg470=
ENST00000688950.1:n.2744C>A
ENST00000689857.1:c.1491C>A	ENSP00000510719.1:p.Arg497=
ENST00000689968.1:c.1644-222C>A	ENSP00000510150.1:n.1644-222C>A
ENST00000690133.1:c.1350C>A	ENSP00000508912.1:p.Arg450=
ENST00000690293.1:c.*1301C>A	ENSP00000509154.1:n.*1301C>A
ENST00000692338.1:c.1350C>A	ENSP00000508700.1:p.Arg450=
ENST00000692468.1:n.1265C>A
ENST00000358741.4:c.1761C>A MANE Select	ENSP00000351591.4:p.Arg587=
ENST00000358741.3:c.1761C>A	ENSP00000351591.3:p.Arg587=
ENST00000374051.7:c.1701C>A	ENSP00000363163.3:p.Arg567=
ENST00000476589.1:n.1265C>A
ENST00000536169.5:c.1641C>A	ENSP00000445298.1:p.Arg547=
ENST00000612180.4:c.*293C>A	ENSP00000479877.1:n.*293C>A
NM_001166660.1:c.1641C>A	NP_001160132.1:p.Arg547=
NM_018977.3:c.1701C>A	NP_061850.2:p.Arg567=
NM_181303.1:c.1761C>A	NP_851820.1:p.Arg587=
XM_005262279.2:c.1703+1511C>A	XP_005262336.1:n.1703+1511C>A
XM_006724662.2:c.1614C>A	XP_006724725.2:p.Arg538=
XM_006724663.2:c.1410C>A	XP_006724726.1:p.Arg470=
XM_011530974.1:c.1410C>A	XP_011529276.1:p.Arg470=
XM_011530975.1:c.1350C>A	XP_011529277.1:p.Arg450=
NM_001321276.1:c.1350C>A	NP_001308205.1:p.Arg450=
XM_006724662.4:c.1614C>A	XP_006724725.2:p.Arg538=
XM_006724663.4:c.1410C>A	XP_006724726.1:p.Arg470=
XM_011530974.3:c.1410C>A	XP_011529276.1:p.Arg470=
XM_017029597.2:c.1703+1511C>A	XP_016885086.1:n.1703+1511C>A
NM_001321276.2:c.1350C>A	NP_001308205.1:p.Arg450=
NM_018977.4:c.1701C>A	NP_061850.2:p.Arg567=
NM_181303.2:c.1761C>A MANE Select	NP_851820.1:p.Arg587=
NM_001166660.2:c.1641C>A	NP_001160132.1:p.Arg547=