Canonical Allele Identifier: CA10573008
Gene: USP9Y HGNC NCBI

Linked Data

dbSNP Id: rs747952575
ExAC: Y:14832489 G / A
MyVariant Identifiers: chrY:g.14832489G>A (hg19) chrY:g.12720556G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12720556G>A , CM000686.2:g.12720556G>A GRCh38
NC_000024.9:g.14832489G>A , CM000686.1:g.14832489G>A GRCh37
NC_000024.8:g.13341883G>A NCBI36
NG_008311.1:g.24330G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.97-33G>A ENSP00000498372.1:n.97-33G>A
ENST00000338981.7:c.97-33G>A MANE Select ENSP00000342812.3:n.97-33G>A
ENST00000426564.6:n.109-33G>A
ENST00000493168.1:n.173-33G>A
NM_004654.3:c.97-33G>A NP_004645.2:n.97-33G>A
XM_011531469.1:c.97-33G>A XP_011529771.1:n.97-33G>A
XM_011531470.1:c.-138-33G>A XP_011529772.1:n.-138-33G>A
XM_017030078.2:c.97-33G>A XP_016885567.1:n.97-33G>A
NM_004654.4:c.97-33G>A MANE Select NP_004645.2:n.97-33G>A
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