Canonical Allele Identifier: CA519989823
Gene: NLGN4Y HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.16936073T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.14824193T>C , CM000686.2:g.14824193T>C GRCh38
NC_000024.9:g.16936073T>C , CM000686.1:g.16936073T>C GRCh37
NC_000024.8:g.15445467T>C NCBI36
NG_028212.1:g.306586T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000684976.1:c.691T>C MANE Select ENSP00000510011.1:p.Leu231=
ENST00000643089.1:c.691T>C ENSP00000496594.1:p.Leu231=
ENST00000339174.9:c.631T>C ENSP00000342535.5:p.Leu211=
ENST00000355905.6:c.631T>C ENSP00000348169.2:p.Leu211=
ENST00000382868.5:c.802T>C ENSP00000372320.1:p.Leu268=
ENST00000382872.5:c.127T>C ENSP00000372325.1:p.Leu43=
ENST00000476359.1:n.1176T>C
NM_001206850.1:c.127T>C NP_001193779.1:p.Leu43=
NM_014893.4:c.631T>C NP_055708.3:p.Leu211=
NR_028319.1:n.1105T>C
NR_046355.1:n.870T>C
XM_006724874.1:c.691T>C XP_006724937.1:p.Leu231=
XM_011531424.1:c.691T>C XP_011529726.1:p.Leu231=
XM_011531425.1:c.691T>C XP_011529727.1:p.Leu231=
XM_011531426.1:c.691T>C XP_011529728.1:p.Leu231=
XM_011531427.1:c.691T>C XP_011529729.1:p.Leu231=
XM_011531428.1:c.691T>C XP_011529730.1:p.Leu231=
XM_011531429.1:c.691T>C XP_011529731.1:p.Leu231=
XM_011531430.1:c.691T>C XP_011529732.1:p.Leu231=
NM_001365584.1:c.691T>C NP_001352513.1:p.Leu231=
NM_001365586.1:c.691T>C NP_001352515.1:p.Leu231=
NM_001365588.1:c.691T>C MANE Select NP_001352517.1:p.Leu231=
NM_001365590.1:c.631T>C NP_001352519.1:p.Leu211=
NM_001365591.1:c.631T>C NP_001352520.1:p.Leu211=
NM_001365592.1:c.631T>C NP_001352521.1:p.Leu211=
NM_001365593.1:c.631T>C NP_001352522.1:p.Leu211=
XM_006724874.2:c.691T>C XP_006724937.1:p.Leu231=
XM_011531427.2:c.691T>C XP_011529729.1:p.Leu231=
XM_011531429.2:c.691T>C XP_011529731.1:p.Leu231=
XM_011531430.2:c.691T>C XP_011529732.1:p.Leu231=
XM_017030036.1:c.631T>C XP_016885525.1:p.Leu211=
XM_017030039.1:c.256T>C XP_016885528.1:p.Leu86=
XM_017030040.1:c.127T>C XP_016885529.1:p.Leu43=
XM_024452490.1:c.691T>C XP_024308258.1:p.Leu231=
NM_001206850.2:c.127T>C NP_001193779.1:p.Leu43=
NM_014893.5:c.631T>C NP_055708.3:p.Leu211=
NR_046355.2:n.870T>C
NM_001394830.1:c.691T>C NP_001381759.1:p.Leu231=
NM_001394831.1:c.631T>C NP_001381760.1:p.Leu211=