Canonical Allele Identifier: CA2766241296

Gene: USP9Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12778323_12778324del , CM000686.2:g.12778323_12778324del	GRCh38
NC_000024.9:g.14890257_14890258del , CM000686.1:g.14890257_14890258del	GRCh37
NC_000024.8:g.13399651_13399652del	NCBI36
NG_008311.1:g.82098_82099del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.2880+64_2880+65del	ENSP00000498372.1:n.2880+64_2880+65del
ENST00000338981.7:c.2880+64_2880+65del MANE Select	ENSP00000342812.3:n.2880+64_2880+65del
ENST00000426564.6:n.2892+64_2892+65del
NM_004654.3:c.2880+64_2880+65del	NP_004645.2:n.2880+64_2880+65del
XM_011531469.1:c.2880+64_2880+65del	XP_011529771.1:n.2880+64_2880+65del
XM_011531470.1:c.2646+64_2646+65del	XP_011529772.1:n.2646+64_2646+65del
XM_017030078.2:c.2895+64_2895+65del	XP_016885567.1:n.2895+64_2895+65del
NM_004654.4:c.2880+64_2880+65del MANE Select	NP_004645.2:n.2880+64_2880+65del