Canonical Allele Identifier: CA414983467

Gene: USP9Y

Linked Data

• dbSNP Id: rs1364135377
• gnomAD v2: Y-14902353-C-T
• MyVariant Identifiers: chrY:g.14902353C>T (hg19) ; chrY:g.12790420C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12790420C>T , CM000686.2:g.12790420C>T	GRCh38
NC_000024.9:g.14902353C>T , CM000686.1:g.14902353C>T	GRCh37
NC_000024.8:g.13411747C>T	NCBI36
NG_008311.1:g.94194C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.3575C>T	ENSP00000498372.1:p.Thr1192Ile
ENST00000338981.7:c.3575C>T MANE Select	ENSP00000342812.3:p.Thr1192Ile
ENST00000426564.6:n.3587C>T
NM_004654.3:c.3575C>T	NP_004645.2:p.Thr1192Ile
XM_011531469.1:c.3575C>T	XP_011529771.1:p.Thr1192Ile
XM_011531470.1:c.3341C>T	XP_011529772.1:p.Thr1114Ile
XM_017030078.2:c.3590C>T	XP_016885567.1:p.Thr1197Ile
NM_004654.4:c.3575C>T MANE Select	NP_004645.2:p.Thr1192Ile