Canonical Allele Identifier: CA2470559195
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12810656T= , CM000686.2:g.12810656T= GRCh38
NC_000024.9:g.14922591T= , CM000686.1:g.14922591T= GRCh37
NC_000024.8:g.13431985T= NCBI36
NG_008311.1:g.114432T=

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.4093-16T= ENSP00000498372.1:n.4093-16T=
ENST00000338981.7:c.4093-16T= MANE Select ENSP00000342812.3:n.4093-16T=
ENST00000426564.6:n.4105-16T=
NM_004654.3:c.4093-16T= NP_004645.2:n.4093-16T=
XM_011531469.1:c.4093-16T= XP_011529771.1:n.4093-16T=
XM_011531470.1:c.3859-16T= XP_011529772.1:n.3859-16T=
XM_017030078.2:c.4108-16T= XP_016885567.1:n.4108-16T=
NM_004654.4:c.4093-16T= MANE Select NP_004645.2:n.4093-16T=