Canonical Allele Identifier: CA414999054
Gene: USP9Y HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.14945718C>A (hg19) chrY:g.12833792C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12833792C>A , CM000686.2:g.12833792C>A GRCh38
NC_000024.9:g.14945718C>A , CM000686.1:g.14945718C>A GRCh37
NC_000024.8:g.13455112C>A NCBI36
NG_008311.1:g.137559C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.5126C>A ENSP00000498372.1:p.Pro1709Gln
ENST00000338981.7:c.5126C>A MANE Select ENSP00000342812.3:p.Pro1709Gln
ENST00000426564.6:n.5138C>A
NM_004654.3:c.5126C>A NP_004645.2:p.Pro1709Gln
XM_011531469.1:c.5126C>A XP_011529771.1:p.Pro1709Gln
XM_011531470.1:c.4892C>A XP_011529772.1:p.Pro1631Gln
XM_017030078.2:c.5141C>A XP_016885567.1:p.Pro1714Gln
NM_004654.4:c.5126C>A MANE Select NP_004645.2:p.Pro1709Gln
Search 100 bp 5'
Search 100 bp 3'