Canonical Allele Identifier: CA2519518938

Gene: NLGN4Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.14529456del , CM000686.2:g.14529456del	GRCh38
NC_000024.9:g.16641336del , CM000686.1:g.16641336del	GRCh37
NC_000024.8:g.15150730del	NCBI36
NG_028212.1:g.11849del

Transcript Alleles

HGVS	Amino-acid change
ENST00000684976.1:c.-112+4748del MANE Select	ENSP00000510011.1:n.-112+4748del
ENST00000643089.1:c.-112+6515del	ENSP00000496594.1:n.-112+6515del
ENST00000645399.1:c.-112+5172del	ENSP00000494046.1:n.-112+5172del
ENST00000339174.9:c.-112+4520del	ENSP00000342535.5:n.-112+4520del
ENST00000355905.6:c.-100+5558del	ENSP00000348169.2:n.-100+5558del
ENST00000382868.5:c.-100+5558del	ENSP00000372320.1:n.-100+5558del
ENST00000382872.5:c.-93+6515del	ENSP00000372325.1:n.-93+6515del
ENST00000471252.1:n.304+6515del
ENST00000476359.1:n.153+5558del
ENST00000481089.1:n.180+4748del
NM_001206850.1:c.-93+6515del	NP_001193779.1:n.-93+6515del
NM_014893.4:c.-100+5558del	NP_055708.3:n.-100+5558del
NR_028319.1:n.363+4520del
NR_046355.1:n.68+5884del
XM_006724874.1:c.-112+5172del	XP_006724937.1:n.-112+5172del
XM_011531424.1:c.-112+4520del	XP_011529726.1:n.-112+4520del
XM_011531425.1:c.-112+4748del	XP_011529727.1:n.-112+4748del
XM_011531426.1:c.-112+6515del	XP_011529728.1:n.-112+6515del
XM_011531428.1:c.-192+4520del	XP_011529730.1:n.-192+4520del
XM_011531430.1:c.-112+4899del	XP_011529732.1:n.-112+4899del
XM_011531431.1:c.-112+4520del	XP_011529733.1:n.-112+4520del
NM_001365584.1:c.-112+4520del	NP_001352513.1:n.-112+4520del
NM_001365586.1:c.-112+6515del	NP_001352515.1:n.-112+6515del
NM_001365588.1:c.-112+4748del MANE Select	NP_001352517.1:n.-112+4748del
NM_001365590.1:c.-319+4520del	NP_001352519.1:n.-319+4520del
NM_001365591.1:c.-112+6515del	NP_001352520.1:n.-112+6515del
NM_001365592.1:c.-112+4748del	NP_001352521.1:n.-112+4748del
NM_001365593.1:c.-112+4899del	NP_001352522.1:n.-112+4899del
XM_006724874.2:c.-112+5172del	XP_006724937.1:n.-112+5172del
XM_011531430.2:c.-112+4899del	XP_011529732.1:n.-112+4899del
XM_017030041.1:c.-112+4748del	XP_016885530.1:n.-112+4748del
NM_001206850.2:c.-93+6515del	NP_001193779.1:n.-93+6515del
NM_014893.5:c.-100+5558del	NP_055708.3:n.-100+5558del
NR_046355.2:n.68+5884del
NM_001394830.1:c.-112+5884del	NP_001381759.1:n.-112+5884del
NM_001394831.1:c.-112+4520del	NP_001381760.1:n.-112+4520del