Canonical Allele Identifier: CA414990058
Gene: USP9Y HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.14922713T>C (hg19) chrY:g.12810778T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12810778T>C , CM000686.2:g.12810778T>C GRCh38
NC_000024.9:g.14922713T>C , CM000686.1:g.14922713T>C GRCh37
NC_000024.8:g.13432107T>C NCBI36
NG_008311.1:g.114554T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.4199T>C ENSP00000498372.1:p.Val1400Ala
ENST00000338981.7:c.4199T>C MANE Select ENSP00000342812.3:p.Val1400Ala
ENST00000426564.6:n.4211T>C
NM_004654.3:c.4199T>C NP_004645.2:p.Val1400Ala
XM_011531469.1:c.4199T>C XP_011529771.1:p.Val1400Ala
XM_011531470.1:c.3965T>C XP_011529772.1:p.Val1322Ala
XM_017030078.2:c.4214T>C XP_016885567.1:p.Val1405Ala
NM_004654.4:c.4199T>C MANE Select NP_004645.2:p.Val1400Ala
Search 100 bp 5'
Search 100 bp 3'