Canonical Allele Identifier: CA10573194

Gene: USP9Y

Linked Data

• dbSNP Id: rs765648757
• ExAC: Y:14889984 G / C
• gnomAD v2: Y-14889984-G-C
• gnomAD v3: Y-12778050-G-C
• gnomAD v4: Y-12778050-G-C
• MyVariant Identifiers: chrY:g.14889984G>C (hg19) ; chrY:g.12778050G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12778050G>C , CM000686.2:g.12778050G>C	GRCh38
NC_000024.9:g.14889984G>C , CM000686.1:g.14889984G>C	GRCh37
NC_000024.8:g.13399378G>C	NCBI36
NG_008311.1:g.81825G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000651177.1:c.2671G>C	ENSP00000498372.1:p.Val891Leu
ENST00000338981.7:c.2671G>C MANE Select	ENSP00000342812.3:p.Val891Leu
ENST00000426564.6:n.2683G>C
NM_004654.3:c.2671G>C	NP_004645.2:p.Val891Leu
XM_011531469.1:c.2671G>C	XP_011529771.1:p.Val891Leu
XM_011531470.1:c.2437G>C	XP_011529772.1:p.Val813Leu
XM_017030078.2:c.2686G>C	XP_016885567.1:p.Val896Leu
NM_004654.4:c.2671G>C MANE Select	NP_004645.2:p.Val891Leu