Canonical Allele Identifier: CA880349625

Gene: NLGN4Y

Linked Data

• dbSNP Id: rs34461404
• gnomAD v3: Y-14697492-TGATAGATAGATA-T
• gnomAD v4: Y-14697492-TGATAGATAGATA-T
• MyVariant Identifiers: chrY:g.16809373_16809384del (hg19) ; chrY:g.14697493_14697504del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.14697527_14697538del , CM000686.2:g.14697527_14697538del	GRCh38
NC_000024.9:g.16809407_16809418del , CM000686.1:g.16809407_16809418del	GRCh37
NC_000024.8:g.15318801_15318812del	NCBI36
NG_028212.1:g.179920_179931del

Transcript Alleles

HGVS	Amino-acid change
ENST00000684976.1:c.473-21932_473-21921del MANE Select	ENSP00000510011.1:n.473-21932_473-21921del
ENST00000643089.1:c.473-21932_473-21921del	ENSP00000496594.1:n.473-21932_473-21921del
ENST00000297967.9:c.473-21932_473-21921del	ENSP00000297967.5:n.473-21932_473-21921del
ENST00000339174.9:c.473-25590_473-25579del	ENSP00000342535.5:n.473-25590_473-25579del
ENST00000355905.6:c.473-25590_473-25579del	ENSP00000348169.2:n.473-25590_473-25579del
ENST00000382868.5:c.473-21932_473-21921del	ENSP00000372320.1:n.473-21932_473-21921del
ENST00000382872.5:c.-92-21932_-92-21921del	ENSP00000372325.1:n.-92-21932_-92-21921del
ENST00000413217.1:c.412-21932_412-21921del
ENST00000476359.1:n.725-21932_725-21921del
NM_001164238.1:c.473-21932_473-21921del	NP_001157710.1:n.473-21932_473-21921del
NM_001206850.1:c.-92-21932_-92-21921del	NP_001193779.1:n.-92-21932_-92-21921del
NM_014893.4:c.473-25590_473-25579del	NP_055708.3:n.473-25590_473-25579del
NR_028319.1:n.947-25590_947-25579del
NR_046355.1:n.652-21932_652-21921del
XM_006724874.1:c.473-21932_473-21921del	XP_006724937.1:n.473-21932_473-21921del
XM_011531424.1:c.473-21932_473-21921del	XP_011529726.1:n.473-21932_473-21921del
XM_011531425.1:c.473-21932_473-21921del	XP_011529727.1:n.473-21932_473-21921del
XM_011531426.1:c.473-21932_473-21921del	XP_011529728.1:n.473-21932_473-21921del
XM_011531427.1:c.473-21932_473-21921del	XP_011529729.1:n.473-21932_473-21921del
XM_011531428.1:c.473-21932_473-21921del	XP_011529730.1:n.473-21932_473-21921del
XM_011531429.1:c.473-21932_473-21921del	XP_011529731.1:n.473-21932_473-21921del
XM_011531430.1:c.473-21932_473-21921del	XP_011529732.1:n.473-21932_473-21921del
XM_011531431.1:c.473-21932_473-21921del	XP_011529733.1:n.473-21932_473-21921del
NM_001365584.1:c.473-21932_473-21921del	NP_001352513.1:n.473-21932_473-21921del
NM_001365586.1:c.473-21932_473-21921del	NP_001352515.1:n.473-21932_473-21921del
NM_001365588.1:c.473-21932_473-21921del MANE Select	NP_001352517.1:n.473-21932_473-21921del
NM_001365590.1:c.473-25590_473-25579del	NP_001352519.1:n.473-25590_473-25579del
NM_001365591.1:c.473-25590_473-25579del	NP_001352520.1:n.473-25590_473-25579del
NM_001365592.1:c.473-25590_473-25579del	NP_001352521.1:n.473-25590_473-25579del
NM_001365593.1:c.473-25590_473-25579del	NP_001352522.1:n.473-25590_473-25579del
XM_006724874.2:c.473-21932_473-21921del	XP_006724937.1:n.473-21932_473-21921del
XM_011531427.2:c.473-21932_473-21921del	XP_011529729.1:n.473-21932_473-21921del
XM_011531429.2:c.473-21932_473-21921del	XP_011529731.1:n.473-21932_473-21921del
XM_011531430.2:c.473-21932_473-21921del	XP_011529732.1:n.473-21932_473-21921del
XM_017030036.1:c.473-25590_473-25579del	XP_016885525.1:n.473-25590_473-25579del
XM_017030039.1:c.-57-3512_-57-3501del	XP_016885528.1:n.-57-3512_-57-3501del
XM_017030041.1:c.473-21932_473-21921del	XP_016885530.1:n.473-21932_473-21921del
XM_024452490.1:c.473-21932_473-21921del	XP_024308258.1:n.473-21932_473-21921del
NM_001206850.2:c.-92-21932_-92-21921del	NP_001193779.1:n.-92-21932_-92-21921del
NM_014893.5:c.473-25590_473-25579del	NP_055708.3:n.473-25590_473-25579del
NR_046355.2:n.652-21932_652-21921del
NM_001394830.1:c.473-21932_473-21921del	NP_001381759.1:n.473-21932_473-21921del
NM_001394831.1:c.473-25590_473-25579del	NP_001381760.1:n.473-25590_473-25579del