Canonical Allele Identifier: CA2766248891
Gene: NLGN4Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.14824109C>T , CM000686.2:g.14824109C>T GRCh38
NC_000024.9:g.16935989C>T , CM000686.1:g.16935989C>T GRCh37
NC_000024.8:g.15445383C>T NCBI36
NG_028212.1:g.306502C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684976.1:c.686-79C>T MANE Select ENSP00000510011.1:n.686-79C>T
ENST00000643089.1:c.686-79C>T ENSP00000496594.1:n.686-79C>T
ENST00000339174.9:c.626-79C>T ENSP00000342535.5:n.626-79C>T
ENST00000355905.6:c.626-79C>T ENSP00000348169.2:n.626-79C>T
ENST00000382868.5:c.797-79C>T ENSP00000372320.1:n.797-79C>T
ENST00000382872.5:c.122-79C>T ENSP00000372325.1:n.122-79C>T
ENST00000476359.1:n.1171-79C>T
NM_001206850.1:c.122-79C>T NP_001193779.1:n.122-79C>T
NM_014893.4:c.626-79C>T NP_055708.3:n.626-79C>T
NR_028319.1:n.1100-79C>T
NR_046355.1:n.865-79C>T
XM_006724874.1:c.686-79C>T XP_006724937.1:n.686-79C>T
XM_011531424.1:c.686-79C>T XP_011529726.1:n.686-79C>T
XM_011531425.1:c.686-79C>T XP_011529727.1:n.686-79C>T
XM_011531426.1:c.686-79C>T XP_011529728.1:n.686-79C>T
XM_011531427.1:c.686-79C>T XP_011529729.1:n.686-79C>T
XM_011531428.1:c.686-79C>T XP_011529730.1:n.686-79C>T
XM_011531429.1:c.686-79C>T XP_011529731.1:n.686-79C>T
XM_011531430.1:c.686-79C>T XP_011529732.1:n.686-79C>T
NM_001365584.1:c.686-79C>T NP_001352513.1:n.686-79C>T
NM_001365586.1:c.686-79C>T NP_001352515.1:n.686-79C>T
NM_001365588.1:c.686-79C>T MANE Select NP_001352517.1:n.686-79C>T
NM_001365590.1:c.626-79C>T NP_001352519.1:n.626-79C>T
NM_001365591.1:c.626-79C>T NP_001352520.1:n.626-79C>T
NM_001365592.1:c.626-79C>T NP_001352521.1:n.626-79C>T
NM_001365593.1:c.626-79C>T NP_001352522.1:n.626-79C>T
XM_006724874.2:c.686-79C>T XP_006724937.1:n.686-79C>T
XM_011531427.2:c.686-79C>T XP_011529729.1:n.686-79C>T
XM_011531429.2:c.686-79C>T XP_011529731.1:n.686-79C>T
XM_011531430.2:c.686-79C>T XP_011529732.1:n.686-79C>T
XM_017030036.1:c.626-79C>T XP_016885525.1:n.626-79C>T
XM_017030039.1:c.251-79C>T XP_016885528.1:n.251-79C>T
XM_017030040.1:c.122-79C>T XP_016885529.1:n.122-79C>T
XM_024452490.1:c.686-79C>T XP_024308258.1:n.686-79C>T
NM_001206850.2:c.122-79C>T NP_001193779.1:n.122-79C>T
NM_014893.5:c.626-79C>T NP_055708.3:n.626-79C>T
NR_046355.2:n.865-79C>T
NM_001394830.1:c.686-79C>T NP_001381759.1:n.686-79C>T
NM_001394831.1:c.626-79C>T NP_001381760.1:n.626-79C>T