Canonical Allele Identifier: CA1139321366

Gene: NLGN4Y

Linked Data

• gnomAD v3: Y-14583887-T-G
• gnomAD v4: Y-14583887-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.14583887T>G , CM000686.2:g.14583887T>G	GRCh38
NC_000024.9:g.16695767T>G , CM000686.1:g.16695767T>G	GRCh37
NC_000024.8:g.15205161T>G	NCBI36
NG_028212.1:g.66280T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000684976.1:c.-111-38122T>G MANE Select	ENSP00000510011.1:n.-111-38122T>G
ENST00000643089.1:c.-111-38122T>G	ENSP00000496594.1:n.-111-38122T>G
ENST00000645399.1:c.-111-38122T>G	ENSP00000494046.1:n.-111-38122T>G
ENST00000339174.9:c.-111-38122T>G	ENSP00000342535.5:n.-111-38122T>G
ENST00000355905.6:c.-99-38134T>G	ENSP00000348169.2:n.-99-38134T>G
ENST00000382868.5:c.-99-38134T>G	ENSP00000372320.1:n.-99-38134T>G
ENST00000382872.5:c.-93+60946T>G	ENSP00000372325.1:n.-93+60946T>G
ENST00000471252.1:n.305-38122T>G
ENST00000476359.1:n.154-38134T>G
ENST00000481089.1:n.181-38122T>G
NM_001206850.1:c.-93+60946T>G	NP_001193779.1:n.-93+60946T>G
NM_014893.4:c.-99-38134T>G	NP_055708.3:n.-99-38134T>G
NR_028319.1:n.364-38122T>G
NR_046355.1:n.69-38122T>G
XM_006724874.1:c.-111-38122T>G	XP_006724937.1:n.-111-38122T>G
XM_011531424.1:c.-111-38122T>G	XP_011529726.1:n.-111-38122T>G
XM_011531425.1:c.-111-38122T>G	XP_011529727.1:n.-111-38122T>G
XM_011531426.1:c.-111-38122T>G	XP_011529728.1:n.-111-38122T>G
XM_011531428.1:c.-112+23216T>G	XP_011529730.1:n.-112+23216T>G
XM_011531430.1:c.-111-38122T>G	XP_011529732.1:n.-111-38122T>G
XM_011531431.1:c.-111-38122T>G	XP_011529733.1:n.-111-38122T>G
NM_001365584.1:c.-111-38122T>G	NP_001352513.1:n.-111-38122T>G
NM_001365586.1:c.-111-38122T>G	NP_001352515.1:n.-111-38122T>G
NM_001365588.1:c.-111-38122T>G MANE Select	NP_001352517.1:n.-111-38122T>G
NM_001365590.1:c.-318-286T>G	NP_001352519.1:n.-318-286T>G
NM_001365591.1:c.-111-38122T>G	NP_001352520.1:n.-111-38122T>G
NM_001365592.1:c.-111-38122T>G	NP_001352521.1:n.-111-38122T>G
NM_001365593.1:c.-111-38122T>G	NP_001352522.1:n.-111-38122T>G
XM_006724874.2:c.-111-38122T>G	XP_006724937.1:n.-111-38122T>G
XM_011531427.2:c.-515T>G	XP_011529729.1:n.-515T>G
XM_011531430.2:c.-111-38122T>G	XP_011529732.1:n.-111-38122T>G
XM_017030041.1:c.-111-38122T>G	XP_016885530.1:n.-111-38122T>G
XM_024452490.1:c.-112+23216T>G	XP_024308258.1:n.-112+23216T>G
NM_001206850.2:c.-93+60946T>G	NP_001193779.1:n.-93+60946T>G
NM_014893.5:c.-99-38134T>G	NP_055708.3:n.-99-38134T>G
NR_046355.2:n.69-38122T>G
NM_001394830.1:c.-111-38122T>G	NP_001381759.1:n.-111-38122T>G
NM_001394831.1:c.-111-38122T>G	NP_001381760.1:n.-111-38122T>G