Canonical Allele Identifier: CA414989921

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14922695A>C (hg19) ; chrY:g.12810760A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12810760A>C , CM000686.2:g.12810760A>C	GRCh38
NC_000024.9:g.14922695A>C , CM000686.1:g.14922695A>C	GRCh37
NC_000024.8:g.13432089A>C	NCBI36
NG_008311.1:g.114536A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.4181A>C	ENSP00000498372.1:p.Asn1394Thr
ENST00000338981.7:c.4181A>C MANE Select	ENSP00000342812.3:p.Asn1394Thr
ENST00000426564.6:n.4193A>C
NM_004654.3:c.4181A>C	NP_004645.2:p.Asn1394Thr
XM_011531469.1:c.4181A>C	XP_011529771.1:p.Asn1394Thr
XM_011531470.1:c.3947A>C	XP_011529772.1:p.Asn1316Thr
XM_017030078.2:c.4196A>C	XP_016885567.1:p.Asn1399Thr
NM_004654.4:c.4181A>C MANE Select	NP_004645.2:p.Asn1394Thr