Canonical Allele Identifier: CA519892161
Gene: USP9Y HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.14890061A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12778127A>C , CM000686.2:g.12778127A>C GRCh38
NC_000024.9:g.14890061A>C , CM000686.1:g.14890061A>C GRCh37
NC_000024.8:g.13399455A>C NCBI36
NG_008311.1:g.81902A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.2748A>C ENSP00000498372.1:p.Val916=
ENST00000338981.7:c.2748A>C MANE Select ENSP00000342812.3:p.Val916=
ENST00000426564.6:n.2760A>C
NM_004654.3:c.2748A>C NP_004645.2:p.Val916=
XM_011531469.1:c.2748A>C XP_011529771.1:p.Val916=
XM_011531470.1:c.2514A>C XP_011529772.1:p.Val838=
XM_017030078.2:c.2763A>C XP_016885567.1:p.Val921=
NM_004654.4:c.2748A>C MANE Select NP_004645.2:p.Val916=
Search 100 bp 5'
Search 100 bp 3'