Canonical Allele Identifier: CA414989149
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12810671G>T , CM000686.2:g.12810671G>T GRCh38
NC_000024.9:g.14922606G>T , CM000686.1:g.14922606G>T GRCh37
NC_000024.8:g.13432000G>T NCBI36
NG_008311.1:g.114447G>T

Transcript Alleles

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