Canonical Allele Identifier: CA337719936

Gene: USP9Y

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12777469G>A , CM000686.2:g.12777469G>A	GRCh38
NC_000024.9:g.14889403G>A , CM000686.1:g.14889403G>A	GRCh37
NC_000024.8:g.13398797G>A	NCBI36
NG_008311.1:g.81244G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.2640-550G>A	ENSP00000498372.1:n.2640-550G>A
ENST00000338981.7:c.2640-550G>A MANE Select	ENSP00000342812.3:n.2640-550G>A
ENST00000426564.6:n.2652-550G>A
NM_004654.3:c.2640-550G>A	NP_004645.2:n.2640-550G>A
XM_011531469.1:c.2640-550G>A	XP_011529771.1:n.2640-550G>A
XM_011531470.1:c.2406-550G>A	XP_011529772.1:n.2406-550G>A
XM_017030078.2:c.2655-550G>A	XP_016885567.1:n.2655-550G>A
NM_004654.4:c.2640-550G>A MANE Select	NP_004645.2:n.2640-550G>A