Canonical Allele Identifier: CA519890892
Gene: USP9Y HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.14922630A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12810695A>G , CM000686.2:g.12810695A>G GRCh38
NC_000024.9:g.14922630A>G , CM000686.1:g.14922630A>G GRCh37
NC_000024.8:g.13432024A>G NCBI36
NG_008311.1:g.114471A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.4116A>G ENSP00000498372.1:p.Lys1372=
ENST00000338981.7:c.4116A>G MANE Select ENSP00000342812.3:p.Lys1372=
ENST00000426564.6:n.4128A>G
NM_004654.3:c.4116A>G NP_004645.2:p.Lys1372=
XM_011531469.1:c.4116A>G XP_011529771.1:p.Lys1372=
XM_011531470.1:c.3882A>G XP_011529772.1:p.Lys1294=
XM_017030078.2:c.4131A>G XP_016885567.1:p.Lys1377=
NM_004654.4:c.4116A>G MANE Select NP_004645.2:p.Lys1372=