Canonical Allele Identifier: CA1139272056

Gene: USP9Y

Linked Data

• gnomAD v3: Y-12833679-CCTT-C
• gnomAD v4: Y-12833679-CCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12833683_12833685del , CM000686.2:g.12833683_12833685del	GRCh38
NC_000024.9:g.14945609_14945611del , CM000686.1:g.14945609_14945611del	GRCh37
NC_000024.8:g.13455003_13455005del	NCBI36
NG_008311.1:g.137450_137452del

Transcript Alleles

HGVS	Amino-acid change
ENST00000651177.1:c.5022-5_5022-3del	ENSP00000498372.1:n.5022-5_5022-3del
ENST00000338981.7:c.5022-5_5022-3del MANE Select	ENSP00000342812.3:n.5022-5_5022-3del
ENST00000426564.6:n.5034-5_5034-3del
NM_004654.3:c.5022-5_5022-3del	NP_004645.2:n.5022-5_5022-3del
XM_011531469.1:c.5022-5_5022-3del	XP_011529771.1:n.5022-5_5022-3del
XM_011531470.1:c.4788-5_4788-3del	XP_011529772.1:n.4788-5_4788-3del
XM_017030078.2:c.5037-5_5037-3del	XP_016885567.1:n.5037-5_5037-3del
NM_004654.4:c.5022-5_5022-3del MANE Select	NP_004645.2:n.5022-5_5022-3del