Canonical Allele Identifier: CA415018982

Gene: NLGN4Y

Linked Data

• MyVariant Identifiers: chrY:g.16936080C>G (hg19) ; chrY:g.14824200C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.14824200C>G , CM000686.2:g.14824200C>G	GRCh38
NC_000024.9:g.16936080C>G , CM000686.1:g.16936080C>G	GRCh37
NC_000024.8:g.15445474C>G	NCBI36
NG_028212.1:g.306593C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684976.1:c.698C>G MANE Select	ENSP00000510011.1:p.Thr233Ser
ENST00000643089.1:c.698C>G	ENSP00000496594.1:p.Thr233Ser
ENST00000339174.9:c.638C>G	ENSP00000342535.5:p.Thr213Ser
ENST00000355905.6:c.638C>G	ENSP00000348169.2:p.Thr213Ser
ENST00000382868.5:c.809C>G	ENSP00000372320.1:p.Thr270Ser
ENST00000382872.5:c.134C>G	ENSP00000372325.1:p.Thr45Ser
ENST00000476359.1:n.1183C>G
NM_001206850.1:c.134C>G	NP_001193779.1:p.Thr45Ser
NM_014893.4:c.638C>G	NP_055708.3:p.Thr213Ser
NR_028319.1:n.1112C>G
NR_046355.1:n.877C>G
XM_006724874.1:c.698C>G	XP_006724937.1:p.Thr233Ser
XM_011531424.1:c.698C>G	XP_011529726.1:p.Thr233Ser
XM_011531425.1:c.698C>G	XP_011529727.1:p.Thr233Ser
XM_011531426.1:c.698C>G	XP_011529728.1:p.Thr233Ser
XM_011531427.1:c.698C>G	XP_011529729.1:p.Thr233Ser
XM_011531428.1:c.698C>G	XP_011529730.1:p.Thr233Ser
XM_011531429.1:c.698C>G	XP_011529731.1:p.Thr233Ser
XM_011531430.1:c.698C>G	XP_011529732.1:p.Thr233Ser
NM_001365584.1:c.698C>G	NP_001352513.1:p.Thr233Ser
NM_001365586.1:c.698C>G	NP_001352515.1:p.Thr233Ser
NM_001365588.1:c.698C>G MANE Select	NP_001352517.1:p.Thr233Ser
NM_001365590.1:c.638C>G	NP_001352519.1:p.Thr213Ser
NM_001365591.1:c.638C>G	NP_001352520.1:p.Thr213Ser
NM_001365592.1:c.638C>G	NP_001352521.1:p.Thr213Ser
NM_001365593.1:c.638C>G	NP_001352522.1:p.Thr213Ser
XM_006724874.2:c.698C>G	XP_006724937.1:p.Thr233Ser
XM_011531427.2:c.698C>G	XP_011529729.1:p.Thr233Ser
XM_011531429.2:c.698C>G	XP_011529731.1:p.Thr233Ser
XM_011531430.2:c.698C>G	XP_011529732.1:p.Thr233Ser
XM_017030036.1:c.638C>G	XP_016885525.1:p.Thr213Ser
XM_017030039.1:c.263C>G	XP_016885528.1:p.Thr88Ser
XM_017030040.1:c.134C>G	XP_016885529.1:p.Thr45Ser
XM_024452490.1:c.698C>G	XP_024308258.1:p.Thr233Ser
NM_001206850.2:c.134C>G	NP_001193779.1:p.Thr45Ser
NM_014893.5:c.638C>G	NP_055708.3:p.Thr213Ser
NR_046355.2:n.877C>G
NM_001394830.1:c.698C>G	NP_001381759.1:p.Thr233Ser
NM_001394831.1:c.638C>G	NP_001381760.1:p.Thr213Ser