Canonical Allele Identifier: CA519895090
Gene: USP9Y HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.14924770A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12812835A>G , CM000686.2:g.12812835A>G GRCh38
NC_000024.9:g.14924770A>G , CM000686.1:g.14924770A>G GRCh37
NC_000024.8:g.13434164A>G NCBI36
NG_008311.1:g.116611A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.4392A>G ENSP00000498372.1:p.Leu1464=
ENST00000338981.7:c.4392A>G MANE Select ENSP00000342812.3:p.Leu1464=
ENST00000426564.6:n.4404A>G
NM_004654.3:c.4392A>G NP_004645.2:p.Leu1464=
XM_011531469.1:c.4392A>G XP_011529771.1:p.Leu1464=
XM_011531470.1:c.4158A>G XP_011529772.1:p.Leu1386=
XM_017030078.2:c.4407A>G XP_016885567.1:p.Leu1469=
NM_004654.4:c.4392A>G MANE Select NP_004645.2:p.Leu1464=
Search 100 bp 5'
Search 100 bp 3'