Canonical Allele Identifier: CA1139320805

Gene: NLGN4Y

Linked Data

• dbSNP Id: rs2080318530
• gnomAD v3: Y-14581177-TTTC-T
• gnomAD v4: Y-14581177-TTTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.14581180_14581182del , CM000686.2:g.14581180_14581182del	GRCh38
NC_000024.9:g.16693060_16693062del , CM000686.1:g.16693060_16693062del	GRCh37
NC_000024.8:g.15202454_15202456del	NCBI36
NG_028212.1:g.63573_63575del

Transcript Alleles

HGVS	Amino-acid change
ENST00000684976.1:c.-111-40829_-111-40827del MANE Select	ENSP00000510011.1:n.-111-40829_-111-40827del
ENST00000643089.1:c.-111-40829_-111-40827del	ENSP00000496594.1:n.-111-40829_-111-40827del
ENST00000645399.1:c.-111-40829_-111-40827del	ENSP00000494046.1:n.-111-40829_-111-40827del
ENST00000339174.9:c.-111-40829_-111-40827del	ENSP00000342535.5:n.-111-40829_-111-40827del
ENST00000355905.6:c.-99-40841_-99-40839del	ENSP00000348169.2:n.-99-40841_-99-40839del
ENST00000382868.5:c.-99-40841_-99-40839del	ENSP00000372320.1:n.-99-40841_-99-40839del
ENST00000382872.5:c.-93+58239_-93+58241del	ENSP00000372325.1:n.-93+58239_-93+58241del
ENST00000471252.1:n.305-40829_305-40827del
ENST00000476359.1:n.154-40841_154-40839del
ENST00000481089.1:n.181-40829_181-40827del
NM_001206850.1:c.-93+58239_-93+58241del	NP_001193779.1:n.-93+58239_-93+58241del
NM_014893.4:c.-99-40841_-99-40839del	NP_055708.3:n.-99-40841_-99-40839del
NR_028319.1:n.364-40829_364-40827del
NR_046355.1:n.69-40829_69-40827del
XM_006724874.1:c.-111-40829_-111-40827del	XP_006724937.1:n.-111-40829_-111-40827del
XM_011531424.1:c.-111-40829_-111-40827del	XP_011529726.1:n.-111-40829_-111-40827del
XM_011531425.1:c.-111-40829_-111-40827del	XP_011529727.1:n.-111-40829_-111-40827del
XM_011531426.1:c.-111-40829_-111-40827del	XP_011529728.1:n.-111-40829_-111-40827del
XM_011531428.1:c.-112+20509_-112+20511del	XP_011529730.1:n.-112+20509_-112+20511del
XM_011531430.1:c.-111-40829_-111-40827del	XP_011529732.1:n.-111-40829_-111-40827del
XM_011531431.1:c.-111-40829_-111-40827del	XP_011529733.1:n.-111-40829_-111-40827del
NM_001365584.1:c.-111-40829_-111-40827del	NP_001352513.1:n.-111-40829_-111-40827del
NM_001365586.1:c.-111-40829_-111-40827del	NP_001352515.1:n.-111-40829_-111-40827del
NM_001365588.1:c.-111-40829_-111-40827del MANE Select	NP_001352517.1:n.-111-40829_-111-40827del
NM_001365590.1:c.-318-2993_-318-2991del	NP_001352519.1:n.-318-2993_-318-2991del
NM_001365591.1:c.-111-40829_-111-40827del	NP_001352520.1:n.-111-40829_-111-40827del
NM_001365592.1:c.-111-40829_-111-40827del	NP_001352521.1:n.-111-40829_-111-40827del
NM_001365593.1:c.-111-40829_-111-40827del	NP_001352522.1:n.-111-40829_-111-40827del
XM_006724874.2:c.-111-40829_-111-40827del	XP_006724937.1:n.-111-40829_-111-40827del
XM_011531430.2:c.-111-40829_-111-40827del	XP_011529732.1:n.-111-40829_-111-40827del
XM_017030041.1:c.-111-40829_-111-40827del	XP_016885530.1:n.-111-40829_-111-40827del
XM_024452490.1:c.-112+20509_-112+20511del	XP_024308258.1:n.-112+20509_-112+20511del
NM_001206850.2:c.-93+58239_-93+58241del	NP_001193779.1:n.-93+58239_-93+58241del
NM_014893.5:c.-99-40841_-99-40839del	NP_055708.3:n.-99-40841_-99-40839del
NR_046355.2:n.69-40829_69-40827del
NM_001394830.1:c.-111-40829_-111-40827del	NP_001381759.1:n.-111-40829_-111-40827del
NM_001394831.1:c.-111-40829_-111-40827del	NP_001381760.1:n.-111-40829_-111-40827del