Canonical Allele Identifier: CA414983357
Gene: USP9Y HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.14902338A>T (hg19) chrY:g.12790405A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12790405A>T , CM000686.2:g.12790405A>T GRCh38
NC_000024.9:g.14902338A>T , CM000686.1:g.14902338A>T GRCh37
NC_000024.8:g.13411732A>T NCBI36
NG_008311.1:g.94179A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.3562-2A>T ENSP00000498372.1:n.3562-2A>T
ENST00000338981.7:c.3562-2A>T MANE Select ENSP00000342812.3:n.3562-2A>T
ENST00000426564.6:n.3574-2A>T
NM_004654.3:c.3562-2A>T NP_004645.2:n.3562-2A>T
XM_011531469.1:c.3562-2A>T XP_011529771.1:n.3562-2A>T
XM_011531470.1:c.3328-2A>T XP_011529772.1:n.3328-2A>T
XM_017030078.2:c.3577-2A>T XP_016885567.1:n.3577-2A>T
NM_004654.4:c.3562-2A>T MANE Select NP_004645.2:n.3562-2A>T
Search 100 bp 5'
Search 100 bp 3'