Canonical Allele Identifier: CA10573065
Gene: USP9Y HGNC NCBI

Linked Data

ClinVar Variation Id: 9757
ClinVar RCV Id: RCV000010411
dbSNP Id: rs778145751
ExAC: Y:14847658 TTAAG / T
gnomAD v2: Y-14847658-TTAAG-T
gnomAD v3: Y-12735724-TTAAG-T
gnomAD v4: Y-12735724-TTAAG-T
MyVariant Identifiers: chrY:g.14847659_14847662del (hg19) chrY:g.12735725_12735728del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12735730_12735733del , CM000686.2:g.12735730_12735733del GRCh38
NC_000024.9:g.14847664_14847667del , CM000686.1:g.14847664_14847667del GRCh37
NC_000024.8:g.13357058_13357061del NCBI36
NG_008311.1:g.39505_39508del

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.773+3_773+6del
ENST00000338981.7:c.773+3_773+6del
ENST00000426564.6:n.785+3_785+6del
NM_004654.3:c.773+3_773+6del
XM_011531469.1:c.773+3_773+6del
XM_011531470.1:c.519+23_519+26del XP_011529772.1:n.519+23_519+26del
XM_017030078.2:c.773+3_773+6del
NM_004654.4:c.773+3_773+6del
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