Canonical Allele Identifier: CA337753022
Gene: NLGN4Y HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs112167022

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.14583872T>C , CM000686.2:g.14583872T>C GRCh38
NC_000024.9:g.16695752T>C , CM000686.1:g.16695752T>C GRCh37
NC_000024.8:g.15205146T>C NCBI36
NG_028212.1:g.66265T>C

Transcript Alleles

HGVS Amino-acid change
NM_001206850.1:c.-93+60931T>C VV NP_001193779.1:p.=
NM_014893.4:c.-99-38149T>C VV NP_055708.3:p.=
NR_028319.1:n.364-38137T>C
NR_046355.1:n.69-38137T>C
XM_006724874.1:c.-111-38137T>C XP_006724937.1:p.=
XM_011531424.1:c.-111-38137T>C XP_011529726.1:p.=
XM_011531425.1:c.-111-38137T>C XP_011529727.1:p.=
XM_011531426.1:c.-111-38137T>C XP_011529728.1:p.=
XM_011531428.1:c.-112+23201T>C XP_011529730.1:p.=
XM_011531430.1:c.-111-38137T>C XP_011529732.1:p.=
XM_011531431.1:c.-111-38137T>C XP_011529733.1:p.=
NM_001365584.1:c.-111-38137T>C VV NP_001352513.1:p.=
NM_001365586.1:c.-111-38137T>C VV NP_001352515.1:p.=
NM_001365588.1:c.-111-38137T>C VV NP_001352517.1:p.=
NM_001365590.1:c.-318-301T>C VV NP_001352519.1:p.=
NM_001365591.1:c.-111-38137T>C VV NP_001352520.1:p.=
NM_001365592.1:c.-111-38137T>C VV NP_001352521.1:p.=
NM_001365593.1:c.-111-38137T>C VV NP_001352522.1:p.=
XM_006724874.2:c.-111-38137T>C
XM_011531427.2:c.-530T>C
XM_011531430.2:c.-111-38137T>C
XM_017030041.1:c.-111-38137T>C XP_016885530.1:p.=
XM_024452490.1:c.-112+23201T>C XP_024308258.1:p.=
ENST00000339174.9:c.-111-38137T>C ENSP00000342535.5:p.=
ENST00000355905.6:c.-99-38149T>C ENSP00000348169.2:p.=
ENST00000382868.5:c.-99-38149T>C ENSP00000372320.1:p.=
ENST00000382872.5:c.-93+60931T>C ENSP00000372325.1:p.=
ENST00000471252.1:n.305-38137T>C
ENST00000476359.1:n.154-38149T>C
ENST00000481089.1:n.181-38137T>C