Canonical Allele Identifier: CA10573190

Gene: USP9Y

Linked Data

• dbSNP Id: rs774838612
• ExAC: Y:14889937 CTTAT / C
• gnomAD v2: Y-14889937-CTTAT-C
• MyVariant Identifiers: chrY:g.14889938_14889941del (hg19) ; chrY:g.12778004_12778007del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12778010_12778013del , CM000686.2:g.12778010_12778013del	GRCh38
NC_000024.9:g.14889944_14889947del , CM000686.1:g.14889944_14889947del	GRCh37
NC_000024.8:g.13399338_13399341del	NCBI36
NG_008311.1:g.81785_81788del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.2640-9_2640-6del	ENSP00000498372.1:n.2640-9_2640-6del
ENST00000338981.7:c.2640-9_2640-6del MANE Select	ENSP00000342812.3:n.2640-9_2640-6del
ENST00000426564.6:n.2652-9_2652-6del
NM_004654.3:c.2640-9_2640-6del	NP_004645.2:n.2640-9_2640-6del
XM_011531469.1:c.2640-9_2640-6del	XP_011529771.1:n.2640-9_2640-6del
XM_011531470.1:c.2406-9_2406-6del	XP_011529772.1:n.2406-9_2406-6del
XM_017030078.2:c.2655-9_2655-6del	XP_016885567.1:n.2655-9_2655-6del
NM_004654.4:c.2640-9_2640-6del MANE Select	NP_004645.2:n.2640-9_2640-6del