Canonical Allele Identifier: CA415009453
Gene: USP9Y HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.14890182A>C (hg19) chrY:g.12778248A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12778248A>C , CM000686.2:g.12778248A>C GRCh38
NC_000024.9:g.14890182A>C , CM000686.1:g.14890182A>C GRCh37
NC_000024.8:g.13399576A>C NCBI36
NG_008311.1:g.82023A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.2869A>C ENSP00000498372.1:p.Lys957Gln
ENST00000338981.7:c.2869A>C MANE Select ENSP00000342812.3:p.Lys957Gln
ENST00000426564.6:n.2881A>C
NM_004654.3:c.2869A>C NP_004645.2:p.Lys957Gln
XM_011531469.1:c.2869A>C XP_011529771.1:p.Lys957Gln
XM_011531470.1:c.2635A>C XP_011529772.1:p.Lys879Gln
XM_017030078.2:c.2884A>C XP_016885567.1:p.Lys962Gln
NM_004654.4:c.2869A>C MANE Select NP_004645.2:p.Lys957Gln
Search 100 bp 5'
Search 100 bp 3'