Canonical Allele Identifier: CA1139769286
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12777955G>T , CM000686.2:g.12777955G>T GRCh38
NC_000024.9:g.14889889G>T , CM000686.1:g.14889889G>T GRCh37
NC_000024.8:g.13399283G>T NCBI36
NG_008311.1:g.81730G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.2640-64G>T ENSP00000498372.1:n.2640-64G>T
ENST00000338981.7:c.2640-64G>T MANE Select ENSP00000342812.3:n.2640-64G>T
ENST00000426564.6:n.2652-64G>T
NM_004654.3:c.2640-64G>T NP_004645.2:n.2640-64G>T
XM_011531469.1:c.2640-64G>T XP_011529771.1:n.2640-64G>T
XM_011531470.1:c.2406-64G>T XP_011529772.1:n.2406-64G>T
XM_017030078.2:c.2655-64G>T XP_016885567.1:n.2655-64G>T
NM_004654.4:c.2640-64G>T MANE Select NP_004645.2:n.2640-64G>T