Canonical Allele Identifier: CA1139167868

Gene: USP9Y

Linked Data

• dbSNP Id: rs2053444110
• gnomAD v3: Y-12727869-G-GT
• gnomAD v4: Y-12727869-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12727870dup , CM000686.2:g.12727870dup	GRCh38
NC_000024.9:g.14839803dup , CM000686.1:g.14839803dup	GRCh37
NC_000024.8:g.13349197dup	NCBI36
NG_008311.1:g.31644dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000651177.1:c.657+1077dup	ENSP00000498372.1:n.657+1077dup
ENST00000338981.7:c.657+1077dup MANE Select	ENSP00000342812.3:n.657+1077dup
ENST00000426564.6:n.669+1077dup
NM_004654.3:c.657+1077dup	NP_004645.2:n.657+1077dup
XM_011531469.1:c.657+1077dup	XP_011529771.1:n.657+1077dup
XM_011531470.1:c.423+1077dup	XP_011529772.1:n.423+1077dup
XM_017030078.2:c.657+1077dup	XP_016885567.1:n.657+1077dup
NM_004654.4:c.657+1077dup MANE Select	NP_004645.2:n.657+1077dup