Canonical Allele Identifier: CA2824942797

Gene: NLGN4Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.14773722_14773723del , CM000686.2:g.14773722_14773723del	GRCh38
NC_000024.9:g.16885602_16885603del , CM000686.1:g.16885602_16885603del	GRCh37
NC_000024.8:g.15394996_15394997del	NCBI36
NG_028212.1:g.256115_256116del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684976.1:c.685+50453_685+50454del MANE Select	ENSP00000510011.1:n.685+50453_685+50454del
ENST00000643089.1:c.685+50453_685+50454del	ENSP00000496594.1:n.685+50453_685+50454del
ENST00000339174.9:c.625+50453_625+50454del	ENSP00000342535.5:n.625+50453_625+50454del
ENST00000355905.6:c.625+50453_625+50454del	ENSP00000348169.2:n.625+50453_625+50454del
ENST00000382868.5:c.796+24993_796+24994del	ENSP00000372320.1:n.796+24993_796+24994del
ENST00000382872.5:c.121+50453_121+50454del	ENSP00000372325.1:n.121+50453_121+50454del
ENST00000476359.1:n.1170+21920_1170+21921del
NM_001206850.1:c.121+50453_121+50454del	NP_001193779.1:n.121+50453_121+50454del
NM_014893.4:c.625+50453_625+50454del	NP_055708.3:n.625+50453_625+50454del
NR_028319.1:n.1099+50453_1099+50454del
NR_046355.1:n.864+50453_864+50454del
XM_006724874.1:c.685+50453_685+50454del	XP_006724937.1:n.685+50453_685+50454del
XM_011531424.1:c.685+50453_685+50454del	XP_011529726.1:n.685+50453_685+50454del
XM_011531425.1:c.685+50453_685+50454del	XP_011529727.1:n.685+50453_685+50454del
XM_011531426.1:c.685+50453_685+50454del	XP_011529728.1:n.685+50453_685+50454del
XM_011531427.1:c.685+50453_685+50454del	XP_011529729.1:n.685+50453_685+50454del
XM_011531428.1:c.685+50453_685+50454del	XP_011529730.1:n.685+50453_685+50454del
XM_011531429.1:c.685+50453_685+50454del	XP_011529731.1:n.685+50453_685+50454del
XM_011531430.1:c.685+50453_685+50454del	XP_011529732.1:n.685+50453_685+50454del
NM_001365584.1:c.685+50453_685+50454del	NP_001352513.1:n.685+50453_685+50454del
NM_001365586.1:c.685+50453_685+50454del	NP_001352515.1:n.685+50453_685+50454del
NM_001365588.1:c.685+50453_685+50454del MANE Select	NP_001352517.1:n.685+50453_685+50454del
NM_001365590.1:c.625+50453_625+50454del	NP_001352519.1:n.625+50453_625+50454del
NM_001365591.1:c.625+50453_625+50454del	NP_001352520.1:n.625+50453_625+50454del
NM_001365592.1:c.625+50453_625+50454del	NP_001352521.1:n.625+50453_625+50454del
NM_001365593.1:c.625+50453_625+50454del	NP_001352522.1:n.625+50453_625+50454del
XM_006724874.2:c.685+50453_685+50454del	XP_006724937.1:n.685+50453_685+50454del
XM_011531427.2:c.685+50453_685+50454del	XP_011529729.1:n.685+50453_685+50454del
XM_011531429.2:c.685+50453_685+50454del	XP_011529731.1:n.685+50453_685+50454del
XM_011531430.2:c.685+50453_685+50454del	XP_011529732.1:n.685+50453_685+50454del
XM_017030036.1:c.625+50453_625+50454del	XP_016885525.1:n.625+50453_625+50454del
XM_017030039.1:c.250+50453_250+50454del	XP_016885528.1:n.250+50453_250+50454del
XM_017030040.1:c.121+50453_121+50454del	XP_016885529.1:n.121+50453_121+50454del
XM_024452490.1:c.685+50453_685+50454del	XP_024308258.1:n.685+50453_685+50454del
NM_001206850.2:c.121+50453_121+50454del	NP_001193779.1:n.121+50453_121+50454del
NM_014893.5:c.625+50453_625+50454del	NP_055708.3:n.625+50453_625+50454del
NR_046355.2:n.864+50453_864+50454del
NM_001394830.1:c.685+50453_685+50454del	NP_001381759.1:n.685+50453_685+50454del
NM_001394831.1:c.625+50453_625+50454del	NP_001381760.1:n.625+50453_625+50454del