Canonical Allele Identifier: CA337752955
Gene: NLGN4Y HGNC NCBI

Linked Data

dbSNP Id: rs185729402

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.14580248_14580249insCCC , CM000686.2:g.14580248_14580249insCCC GRCh38
NC_000024.9:g.16692128_16692129insCCC , CM000686.1:g.16692128_16692129insCCC GRCh37
NC_000024.8:g.15201522_15201523insCCC NCBI36
NG_028212.1:g.62641_62642insCCC

Transcript Alleles

HGVS Amino-acid change
ENST00000684976.1:c.-111-41761_-111-41760insCCC MANE Select ENSP00000510011.1:n.-111-41761_-111-41760...
ENST00000643089.1:c.-111-41761_-111-41760insCCC ENSP00000496594.1:n.-111-41761_-111-41760...
ENST00000645399.1:c.-111-41761_-111-41760insCCC ENSP00000494046.1:n.-111-41761_-111-41760...
ENST00000339174.9:c.-111-41761_-111-41760insCCC ENSP00000342535.5:n.-111-41761_-111-41760...
ENST00000355905.6:c.-99-41773_-99-41772insCCC ENSP00000348169.2:n.-99-41773_-99-41772in...
ENST00000382868.5:c.-99-41773_-99-41772insCCC ENSP00000372320.1:n.-99-41773_-99-41772in...
ENST00000382872.5:c.-93+57307_-93+57308insCCC ENSP00000372325.1:n.-93+57307_-93+57308in...
ENST00000471252.1:n.305-41761_305-41760insCCC
ENST00000476359.1:n.154-41773_154-41772insCCC
ENST00000481089.1:n.181-41761_181-41760insCCC
NM_001206850.1:c.-93+57307_-93+57308insCCC NP_001193779.1:n.-93+57307_-93+57308insCC...
NM_014893.4:c.-99-41773_-99-41772insCCC NP_055708.3:n.-99-41773_-99-41772insCCC
NR_028319.1:n.364-41761_364-41760insCCC
NR_046355.1:n.69-41761_69-41760insCCC
XM_006724874.1:c.-111-41761_-111-41760insCCC XP_006724937.1:n.-111-41761_-111-41760ins...
XM_011531424.1:c.-111-41761_-111-41760insCCC XP_011529726.1:n.-111-41761_-111-41760ins...
XM_011531425.1:c.-111-41761_-111-41760insCCC XP_011529727.1:n.-111-41761_-111-41760ins...
XM_011531426.1:c.-111-41761_-111-41760insCCC XP_011529728.1:n.-111-41761_-111-41760ins...
XM_011531428.1:c.-112+19577_-112+19578insCCC XP_011529730.1:n.-112+19577_-112+19578ins...
XM_011531430.1:c.-111-41761_-111-41760insCCC XP_011529732.1:n.-111-41761_-111-41760ins...
XM_011531431.1:c.-111-41761_-111-41760insCCC XP_011529733.1:n.-111-41761_-111-41760ins...
NM_001365584.1:c.-111-41761_-111-41760insCCC NP_001352513.1:n.-111-41761_-111-41760ins...
NM_001365586.1:c.-111-41761_-111-41760insCCC NP_001352515.1:n.-111-41761_-111-41760ins...
NM_001365588.1:c.-111-41761_-111-41760insCCC MANE Select NP_001352517.1:n.-111-41761_-111-41760ins...
NM_001365590.1:c.-318-3925_-318-3924insCCC NP_001352519.1:n.-318-3925_-318-3924insCC...
NM_001365591.1:c.-111-41761_-111-41760insCCC NP_001352520.1:n.-111-41761_-111-41760ins...
NM_001365592.1:c.-111-41761_-111-41760insCCC NP_001352521.1:n.-111-41761_-111-41760ins...
NM_001365593.1:c.-111-41761_-111-41760insCCC NP_001352522.1:n.-111-41761_-111-41760ins...
XM_006724874.2:c.-111-41761_-111-41760insCCC XP_006724937.1:n.-111-41761_-111-41760ins...
XM_011531430.2:c.-111-41761_-111-41760insCCC XP_011529732.1:n.-111-41761_-111-41760ins...
XM_017030041.1:c.-111-41761_-111-41760insCCC XP_016885530.1:n.-111-41761_-111-41760ins...
XM_024452490.1:c.-112+19577_-112+19578insCCC XP_024308258.1:n.-112+19577_-112+19578ins...
NM_001206850.2:c.-93+57307_-93+57308insCCC NP_001193779.1:n.-93+57307_-93+57308insCC...
NM_014893.5:c.-99-41773_-99-41772insCCC NP_055708.3:n.-99-41773_-99-41772insCCC
NR_046355.2:n.69-41761_69-41760insCCC
NM_001394830.1:c.-111-41761_-111-41760insCCC NP_001381759.1:n.-111-41761_-111-41760ins...
NM_001394831.1:c.-111-41761_-111-41760insCCC NP_001381760.1:n.-111-41761_-111-41760ins...