Canonical Allele Identifier: CA1139183259

Gene: USP9Y

Linked Data

• dbSNP Id: rs2053495230
• gnomAD v3: Y-12778365-G-T
• gnomAD v4: Y-12778365-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12778365G>T , CM000686.2:g.12778365G>T	GRCh38
NC_000024.9:g.14890299G>T , CM000686.1:g.14890299G>T	GRCh37
NC_000024.8:g.13399693G>T	NCBI36
NG_008311.1:g.82140G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.2880+106G>T	ENSP00000498372.1:n.2880+106G>T
ENST00000338981.7:c.2880+106G>T MANE Select	ENSP00000342812.3:n.2880+106G>T
ENST00000426564.6:n.2892+106G>T
NM_004654.3:c.2880+106G>T	NP_004645.2:n.2880+106G>T
XM_011531469.1:c.2880+106G>T	XP_011529771.1:n.2880+106G>T
XM_011531470.1:c.2646+106G>T	XP_011529772.1:n.2646+106G>T
XM_017030078.2:c.2895+106G>T	XP_016885567.1:n.2895+106G>T
NM_004654.4:c.2880+106G>T MANE Select	NP_004645.2:n.2880+106G>T