Canonical Allele Identifier: CA1139320850

Gene: NLGN4Y

Linked Data

• dbSNP Id: rs2080319184
• gnomAD v3: Y-14581265-T-TC
• gnomAD v4: Y-14581265-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.14581265_14581266insC , CM000686.2:g.14581265_14581266insC	GRCh38
NC_000024.9:g.16693145_16693146insC , CM000686.1:g.16693145_16693146insC	GRCh37
NC_000024.8:g.15202539_15202540insC	NCBI36
NG_028212.1:g.63658_63659insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684976.1:c.-111-40744_-111-40743insC MANE Select	ENSP00000510011.1:n.-111-40744_-111-40743insC
ENST00000643089.1:c.-111-40744_-111-40743insC	ENSP00000496594.1:n.-111-40744_-111-40743insC
ENST00000645399.1:c.-111-40744_-111-40743insC	ENSP00000494046.1:n.-111-40744_-111-40743insC
ENST00000339174.9:c.-111-40744_-111-40743insC	ENSP00000342535.5:n.-111-40744_-111-40743insC
ENST00000355905.6:c.-99-40756_-99-40755insC	ENSP00000348169.2:n.-99-40756_-99-40755insC
ENST00000382868.5:c.-99-40756_-99-40755insC	ENSP00000372320.1:n.-99-40756_-99-40755insC
ENST00000382872.5:c.-93+58324_-93+58325insC	ENSP00000372325.1:n.-93+58324_-93+58325insC
ENST00000471252.1:n.305-40744_305-40743insC
ENST00000476359.1:n.154-40756_154-40755insC
ENST00000481089.1:n.181-40744_181-40743insC
NM_001206850.1:c.-93+58324_-93+58325insC	NP_001193779.1:n.-93+58324_-93+58325insC
NM_014893.4:c.-99-40756_-99-40755insC	NP_055708.3:n.-99-40756_-99-40755insC
NR_028319.1:n.364-40744_364-40743insC
NR_046355.1:n.69-40744_69-40743insC
XM_006724874.1:c.-111-40744_-111-40743insC	XP_006724937.1:n.-111-40744_-111-40743insC
XM_011531424.1:c.-111-40744_-111-40743insC	XP_011529726.1:n.-111-40744_-111-40743insC
XM_011531425.1:c.-111-40744_-111-40743insC	XP_011529727.1:n.-111-40744_-111-40743insC
XM_011531426.1:c.-111-40744_-111-40743insC	XP_011529728.1:n.-111-40744_-111-40743insC
XM_011531428.1:c.-112+20594_-112+20595insC	XP_011529730.1:n.-112+20594_-112+20595insC
XM_011531430.1:c.-111-40744_-111-40743insC	XP_011529732.1:n.-111-40744_-111-40743insC
XM_011531431.1:c.-111-40744_-111-40743insC	XP_011529733.1:n.-111-40744_-111-40743insC
NM_001365584.1:c.-111-40744_-111-40743insC	NP_001352513.1:n.-111-40744_-111-40743insC
NM_001365586.1:c.-111-40744_-111-40743insC	NP_001352515.1:n.-111-40744_-111-40743insC
NM_001365588.1:c.-111-40744_-111-40743insC MANE Select	NP_001352517.1:n.-111-40744_-111-40743insC
NM_001365590.1:c.-318-2908_-318-2907insC	NP_001352519.1:n.-318-2908_-318-2907insC
NM_001365591.1:c.-111-40744_-111-40743insC	NP_001352520.1:n.-111-40744_-111-40743insC
NM_001365592.1:c.-111-40744_-111-40743insC	NP_001352521.1:n.-111-40744_-111-40743insC
NM_001365593.1:c.-111-40744_-111-40743insC	NP_001352522.1:n.-111-40744_-111-40743insC
XM_006724874.2:c.-111-40744_-111-40743insC	XP_006724937.1:n.-111-40744_-111-40743insC
XM_011531430.2:c.-111-40744_-111-40743insC	XP_011529732.1:n.-111-40744_-111-40743insC
XM_017030041.1:c.-111-40744_-111-40743insC	XP_016885530.1:n.-111-40744_-111-40743insC
XM_024452490.1:c.-112+20594_-112+20595insC	XP_024308258.1:n.-112+20594_-112+20595insC
NM_001206850.2:c.-93+58324_-93+58325insC	NP_001193779.1:n.-93+58324_-93+58325insC
NM_014893.5:c.-99-40756_-99-40755insC	NP_055708.3:n.-99-40756_-99-40755insC
NR_046355.2:n.69-40744_69-40743insC
NM_001394830.1:c.-111-40744_-111-40743insC	NP_001381759.1:n.-111-40744_-111-40743insC
NM_001394831.1:c.-111-40744_-111-40743insC	NP_001381760.1:n.-111-40744_-111-40743insC