Canonical Allele Identifier: CA414999063

Gene: USP9Y

Linked Data

• dbSNP Id: rs1378284106
• gnomAD v2: Y-14945720-G-T
• MyVariant Identifiers: chrY:g.14945720G>T (hg19) ; chrY:g.12833794G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12833794G>T , CM000686.2:g.12833794G>T	GRCh38
NC_000024.9:g.14945720G>T , CM000686.1:g.14945720G>T	GRCh37
NC_000024.8:g.13455114G>T	NCBI36
NG_008311.1:g.137561G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000651177.1:c.5128G>T	ENSP00000498372.1:p.Ala1710Ser
ENST00000338981.7:c.5128G>T MANE Select	ENSP00000342812.3:p.Ala1710Ser
ENST00000426564.6:n.5140G>T
NM_004654.3:c.5128G>T	NP_004645.2:p.Ala1710Ser
XM_011531469.1:c.5128G>T	XP_011529771.1:p.Ala1710Ser
XM_011531470.1:c.4894G>T	XP_011529772.1:p.Ala1632Ser
XM_017030078.2:c.5143G>T	XP_016885567.1:p.Ala1715Ser
NM_004654.4:c.5128G>T MANE Select	NP_004645.2:p.Ala1710Ser