Canonical Allele Identifier: CA10573062

Gene: USP9Y

Linked Data

• dbSNP Id: rs759180265
• ExAC: Y:14847635 T / C
• gnomAD v2: Y-14847635-T-C
• MyVariant Identifiers: chrY:g.14847635T>C (hg19) ; chrY:g.12735701T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12735701T>C , CM000686.2:g.12735701T>C	GRCh38
NC_000024.9:g.14847635T>C , CM000686.1:g.14847635T>C	GRCh37
NC_000024.8:g.13357029T>C	NCBI36
NG_008311.1:g.39476T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.747T>C	ENSP00000498372.1:p.Asn249=
ENST00000338981.7:c.747T>C MANE Select	ENSP00000342812.3:p.Asn249=
ENST00000426564.6:n.759T>C
NM_004654.3:c.747T>C	NP_004645.2:p.Asn249=
XM_011531469.1:c.747T>C	XP_011529771.1:p.Asn249=
XM_011531470.1:c.513T>C	XP_011529772.1:p.Asn171=
XM_017030078.2:c.747T>C	XP_016885567.1:p.Asn249=
NM_004654.4:c.747T>C MANE Select	NP_004645.2:p.Asn249=