Canonical Allele Identifier: CA337756450
Gene: NLGN4Y HGNC NCBI

Linked Data

dbSNP Id: rs112045755
gnomAD v3: Y-14753877-G-C
gnomAD v4: Y-14753877-G-C
MyVariant Identifiers: chrY:g.16865757G>C (hg19) chrY:g.14753877G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.14753877G>C , CM000686.2:g.14753877G>C GRCh38
NC_000024.9:g.16865757G>C , CM000686.1:g.16865757G>C GRCh37
NC_000024.8:g.15375151G>C NCBI36
NG_028212.1:g.236270G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000684976.1:c.685+30608G>C MANE Select ENSP00000510011.1:n.685+30608G>C
ENST00000643089.1:c.685+30608G>C ENSP00000496594.1:n.685+30608G>C
ENST00000339174.9:c.625+30608G>C ENSP00000342535.5:n.625+30608G>C
ENST00000355905.6:c.625+30608G>C ENSP00000348169.2:n.625+30608G>C
ENST00000382868.5:c.796+5148G>C ENSP00000372320.1:n.796+5148G>C
ENST00000382872.5:c.121+30608G>C ENSP00000372325.1:n.121+30608G>C
ENST00000476359.1:n.1170+2075G>C
NM_001206850.1:c.121+30608G>C NP_001193779.1:n.121+30608G>C
NM_014893.4:c.625+30608G>C NP_055708.3:n.625+30608G>C
NR_028319.1:n.1099+30608G>C
NR_046355.1:n.864+30608G>C
XM_006724874.1:c.685+30608G>C XP_006724937.1:n.685+30608G>C
XM_011531424.1:c.685+30608G>C XP_011529726.1:n.685+30608G>C
XM_011531425.1:c.685+30608G>C XP_011529727.1:n.685+30608G>C
XM_011531426.1:c.685+30608G>C XP_011529728.1:n.685+30608G>C
XM_011531427.1:c.685+30608G>C XP_011529729.1:n.685+30608G>C
XM_011531428.1:c.685+30608G>C XP_011529730.1:n.685+30608G>C
XM_011531429.1:c.685+30608G>C XP_011529731.1:n.685+30608G>C
XM_011531430.1:c.685+30608G>C XP_011529732.1:n.685+30608G>C
NM_001365584.1:c.685+30608G>C NP_001352513.1:n.685+30608G>C
NM_001365586.1:c.685+30608G>C NP_001352515.1:n.685+30608G>C
NM_001365588.1:c.685+30608G>C MANE Select NP_001352517.1:n.685+30608G>C
NM_001365590.1:c.625+30608G>C NP_001352519.1:n.625+30608G>C
NM_001365591.1:c.625+30608G>C NP_001352520.1:n.625+30608G>C
NM_001365592.1:c.625+30608G>C NP_001352521.1:n.625+30608G>C
NM_001365593.1:c.625+30608G>C NP_001352522.1:n.625+30608G>C
XM_006724874.2:c.685+30608G>C XP_006724937.1:n.685+30608G>C
XM_011531427.2:c.685+30608G>C XP_011529729.1:n.685+30608G>C
XM_011531429.2:c.685+30608G>C XP_011529731.1:n.685+30608G>C
XM_011531430.2:c.685+30608G>C XP_011529732.1:n.685+30608G>C
XM_017030036.1:c.625+30608G>C XP_016885525.1:n.625+30608G>C
XM_017030039.1:c.250+30608G>C XP_016885528.1:n.250+30608G>C
XM_017030040.1:c.121+30608G>C XP_016885529.1:n.121+30608G>C
XM_024452490.1:c.685+30608G>C XP_024308258.1:n.685+30608G>C
NM_001206850.2:c.121+30608G>C NP_001193779.1:n.121+30608G>C
NM_014893.5:c.625+30608G>C NP_055708.3:n.625+30608G>C
NR_046355.2:n.864+30608G>C
NM_001394830.1:c.685+30608G>C NP_001381759.1:n.685+30608G>C
NM_001394831.1:c.625+30608G>C NP_001381760.1:n.625+30608G>C
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