Canonical Allele Identifier: CA2505850973

Gene: NLGN4Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.14529603G>T , CM000686.2:g.14529603G>T	GRCh38
NC_000024.9:g.16641483G>T , CM000686.1:g.16641483G>T	GRCh37
NC_000024.8:g.15150877G>T	NCBI36
NG_028212.1:g.11996G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684976.1:c.-112+4895G>T MANE Select	ENSP00000510011.1:n.-112+4895G>T
ENST00000643089.1:c.-112+6662G>T	ENSP00000496594.1:n.-112+6662G>T
ENST00000645399.1:c.-112+5319G>T	ENSP00000494046.1:n.-112+5319G>T
ENST00000339174.9:c.-112+4667G>T	ENSP00000342535.5:n.-112+4667G>T
ENST00000355905.6:c.-100+5705G>T	ENSP00000348169.2:n.-100+5705G>T
ENST00000382868.5:c.-100+5705G>T	ENSP00000372320.1:n.-100+5705G>T
ENST00000382872.5:c.-93+6662G>T	ENSP00000372325.1:n.-93+6662G>T
ENST00000471252.1:n.304+6662G>T
ENST00000476359.1:n.153+5705G>T
ENST00000481089.1:n.180+4895G>T
NM_001206850.1:c.-93+6662G>T	NP_001193779.1:n.-93+6662G>T
NM_014893.4:c.-100+5705G>T	NP_055708.3:n.-100+5705G>T
NR_028319.1:n.363+4667G>T
NR_046355.1:n.68+6031G>T
XM_006724874.1:c.-112+5319G>T	XP_006724937.1:n.-112+5319G>T
XM_011531424.1:c.-112+4667G>T	XP_011529726.1:n.-112+4667G>T
XM_011531425.1:c.-112+4895G>T	XP_011529727.1:n.-112+4895G>T
XM_011531426.1:c.-112+6662G>T	XP_011529728.1:n.-112+6662G>T
XM_011531428.1:c.-192+4667G>T	XP_011529730.1:n.-192+4667G>T
XM_011531430.1:c.-112+5046G>T	XP_011529732.1:n.-112+5046G>T
XM_011531431.1:c.-112+4667G>T	XP_011529733.1:n.-112+4667G>T
NM_001365584.1:c.-112+4667G>T	NP_001352513.1:n.-112+4667G>T
NM_001365586.1:c.-112+6662G>T	NP_001352515.1:n.-112+6662G>T
NM_001365588.1:c.-112+4895G>T MANE Select	NP_001352517.1:n.-112+4895G>T
NM_001365590.1:c.-319+4667G>T	NP_001352519.1:n.-319+4667G>T
NM_001365591.1:c.-112+6662G>T	NP_001352520.1:n.-112+6662G>T
NM_001365592.1:c.-112+4895G>T	NP_001352521.1:n.-112+4895G>T
NM_001365593.1:c.-112+5046G>T	NP_001352522.1:n.-112+5046G>T
XM_006724874.2:c.-112+5319G>T	XP_006724937.1:n.-112+5319G>T
XM_011531430.2:c.-112+5046G>T	XP_011529732.1:n.-112+5046G>T
XM_017030041.1:c.-112+4895G>T	XP_016885530.1:n.-112+4895G>T
NM_001206850.2:c.-93+6662G>T	NP_001193779.1:n.-93+6662G>T
NM_014893.5:c.-100+5705G>T	NP_055708.3:n.-100+5705G>T
NR_046355.2:n.68+6031G>T
NM_001394830.1:c.-112+6031G>T	NP_001381759.1:n.-112+6031G>T
NM_001394831.1:c.-112+4667G>T	NP_001381760.1:n.-112+4667G>T