Canonical Allele Identifier: CA2526183227
Gene: NLGN4Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.14526998_14527007del , CM000686.2:g.14526998_14527007del GRCh38
NC_000024.9:g.16638878_16638887del , CM000686.1:g.16638878_16638887del GRCh37
NC_000024.8:g.15148272_15148281del NCBI36
NG_028212.1:g.9391_9400del

Transcript Alleles

HGVS Amino-acid change
ENST00000684976.1:c.-112+2290_-112+2299del MANE Select ENSP00000510011.1:n.-112+2290_-112+2299de...
ENST00000643089.1:c.-112+4057_-112+4066del ENSP00000496594.1:n.-112+4057_-112+4066de...
ENST00000645399.1:c.-112+2714_-112+2723del ENSP00000494046.1:n.-112+2714_-112+2723de...
ENST00000339174.9:c.-112+2062_-112+2071del ENSP00000342535.5:n.-112+2062_-112+2071de...
ENST00000355905.6:c.-100+3100_-100+3109del ENSP00000348169.2:n.-100+3100_-100+3109de...
ENST00000382868.5:c.-100+3100_-100+3109del ENSP00000372320.1:n.-100+3100_-100+3109de...
ENST00000382872.5:c.-93+4057_-93+4066del ENSP00000372325.1:n.-93+4057_-93+4066del
ENST00000471252.1:n.304+4057_304+4066del
ENST00000476359.1:n.153+3100_153+3109del
ENST00000481089.1:n.180+2290_180+2299del
NM_001206850.1:c.-93+4057_-93+4066del NP_001193779.1:n.-93+4057_-93+4066del
NM_014893.4:c.-100+3100_-100+3109del NP_055708.3:n.-100+3100_-100+3109del
NR_028319.1:n.363+2062_363+2071del
NR_046355.1:n.68+3426_68+3435del
XM_006724874.1:c.-112+2714_-112+2723del XP_006724937.1:n.-112+2714_-112+2723del
XM_011531424.1:c.-112+2062_-112+2071del XP_011529726.1:n.-112+2062_-112+2071del
XM_011531425.1:c.-112+2290_-112+2299del XP_011529727.1:n.-112+2290_-112+2299del
XM_011531426.1:c.-112+4057_-112+4066del XP_011529728.1:n.-112+4057_-112+4066del
XM_011531428.1:c.-192+2062_-192+2071del XP_011529730.1:n.-192+2062_-192+2071del
XM_011531430.1:c.-112+2441_-112+2450del XP_011529732.1:n.-112+2441_-112+2450del
XM_011531431.1:c.-112+2062_-112+2071del XP_011529733.1:n.-112+2062_-112+2071del
NM_001365584.1:c.-112+2062_-112+2071del NP_001352513.1:n.-112+2062_-112+2071del
NM_001365586.1:c.-112+4057_-112+4066del NP_001352515.1:n.-112+4057_-112+4066del
NM_001365588.1:c.-112+2290_-112+2299del MANE Select NP_001352517.1:n.-112+2290_-112+2299del
NM_001365590.1:c.-319+2062_-319+2071del NP_001352519.1:n.-319+2062_-319+2071del
NM_001365591.1:c.-112+4057_-112+4066del NP_001352520.1:n.-112+4057_-112+4066del
NM_001365592.1:c.-112+2290_-112+2299del NP_001352521.1:n.-112+2290_-112+2299del
NM_001365593.1:c.-112+2441_-112+2450del NP_001352522.1:n.-112+2441_-112+2450del
XM_006724874.2:c.-112+2714_-112+2723del XP_006724937.1:n.-112+2714_-112+2723del
XM_011531430.2:c.-112+2441_-112+2450del XP_011529732.1:n.-112+2441_-112+2450del
XM_017030041.1:c.-112+2290_-112+2299del XP_016885530.1:n.-112+2290_-112+2299del
NM_001206850.2:c.-93+4057_-93+4066del NP_001193779.1:n.-93+4057_-93+4066del
NM_014893.5:c.-100+3100_-100+3109del NP_055708.3:n.-100+3100_-100+3109del
NR_046355.2:n.68+3426_68+3435del
NM_001394830.1:c.-112+3426_-112+3435del NP_001381759.1:n.-112+3426_-112+3435del
NM_001394831.1:c.-112+2062_-112+2071del NP_001381760.1:n.-112+2062_-112+2071del