Canonical Allele Identifier: CA414990009

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14922706G>C (hg19) ; chrY:g.12810771G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12810771G>C , CM000686.2:g.12810771G>C	GRCh38
NC_000024.9:g.14922706G>C , CM000686.1:g.14922706G>C	GRCh37
NC_000024.8:g.13432100G>C	NCBI36
NG_008311.1:g.114547G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.4192G>C	ENSP00000498372.1:p.Ala1398Pro
ENST00000338981.7:c.4192G>C MANE Select	ENSP00000342812.3:p.Ala1398Pro
ENST00000426564.6:n.4204G>C
NM_004654.3:c.4192G>C	NP_004645.2:p.Ala1398Pro
XM_011531469.1:c.4192G>C	XP_011529771.1:p.Ala1398Pro
XM_011531470.1:c.3958G>C	XP_011529772.1:p.Ala1320Pro
XM_017030078.2:c.4207G>C	XP_016885567.1:p.Ala1403Pro
NM_004654.4:c.4192G>C MANE Select	NP_004645.2:p.Ala1398Pro