Canonical Allele Identifier: CA415018973

Gene: NLGN4Y

Linked Data

• MyVariant Identifiers: chrY:g.16936077G>C (hg19) ; chrY:g.14824197G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.14824197G>C , CM000686.2:g.14824197G>C	GRCh38
NC_000024.9:g.16936077G>C , CM000686.1:g.16936077G>C	GRCh37
NC_000024.8:g.15445471G>C	NCBI36
NG_028212.1:g.306590G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684976.1:c.695G>C MANE Select	ENSP00000510011.1:p.Ser232Thr
ENST00000643089.1:c.695G>C	ENSP00000496594.1:p.Ser232Thr
ENST00000339174.9:c.635G>C	ENSP00000342535.5:p.Ser212Thr
ENST00000355905.6:c.635G>C	ENSP00000348169.2:p.Ser212Thr
ENST00000382868.5:c.806G>C	ENSP00000372320.1:p.Ser269Thr
ENST00000382872.5:c.131G>C	ENSP00000372325.1:p.Ser44Thr
ENST00000476359.1:n.1180G>C
NM_001206850.1:c.131G>C	NP_001193779.1:p.Ser44Thr
NM_014893.4:c.635G>C	NP_055708.3:p.Ser212Thr
NR_028319.1:n.1109G>C
NR_046355.1:n.874G>C
XM_006724874.1:c.695G>C	XP_006724937.1:p.Ser232Thr
XM_011531424.1:c.695G>C	XP_011529726.1:p.Ser232Thr
XM_011531425.1:c.695G>C	XP_011529727.1:p.Ser232Thr
XM_011531426.1:c.695G>C	XP_011529728.1:p.Ser232Thr
XM_011531427.1:c.695G>C	XP_011529729.1:p.Ser232Thr
XM_011531428.1:c.695G>C	XP_011529730.1:p.Ser232Thr
XM_011531429.1:c.695G>C	XP_011529731.1:p.Ser232Thr
XM_011531430.1:c.695G>C	XP_011529732.1:p.Ser232Thr
NM_001365584.1:c.695G>C	NP_001352513.1:p.Ser232Thr
NM_001365586.1:c.695G>C	NP_001352515.1:p.Ser232Thr
NM_001365588.1:c.695G>C MANE Select	NP_001352517.1:p.Ser232Thr
NM_001365590.1:c.635G>C	NP_001352519.1:p.Ser212Thr
NM_001365591.1:c.635G>C	NP_001352520.1:p.Ser212Thr
NM_001365592.1:c.635G>C	NP_001352521.1:p.Ser212Thr
NM_001365593.1:c.635G>C	NP_001352522.1:p.Ser212Thr
XM_006724874.2:c.695G>C	XP_006724937.1:p.Ser232Thr
XM_011531427.2:c.695G>C	XP_011529729.1:p.Ser232Thr
XM_011531429.2:c.695G>C	XP_011529731.1:p.Ser232Thr
XM_011531430.2:c.695G>C	XP_011529732.1:p.Ser232Thr
XM_017030036.1:c.635G>C	XP_016885525.1:p.Ser212Thr
XM_017030039.1:c.260G>C	XP_016885528.1:p.Ser87Thr
XM_017030040.1:c.131G>C	XP_016885529.1:p.Ser44Thr
XM_024452490.1:c.695G>C	XP_024308258.1:p.Ser232Thr
NM_001206850.2:c.131G>C	NP_001193779.1:p.Ser44Thr
NM_014893.5:c.635G>C	NP_055708.3:p.Ser212Thr
NR_046355.2:n.874G>C
NM_001394830.1:c.695G>C	NP_001381759.1:p.Ser232Thr
NM_001394831.1:c.635G>C	NP_001381760.1:p.Ser212Thr