Canonical Allele Identifier: CA414981969
Gene: USP9Y HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.14838706T>G (hg19) chrY:g.12726773T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12726773T>G , CM000686.2:g.12726773T>G GRCh38
NC_000024.9:g.14838706T>G , CM000686.1:g.14838706T>G GRCh37
NC_000024.8:g.13348100T>G NCBI36
NG_008311.1:g.30547T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.637T>G ENSP00000498372.1:p.Ser213Ala
ENST00000338981.7:c.637T>G MANE Select ENSP00000342812.3:p.Ser213Ala
ENST00000426564.6:n.649T>G
NM_004654.3:c.637T>G NP_004645.2:p.Ser213Ala
XM_011531469.1:c.637T>G XP_011529771.1:p.Ser213Ala
XM_011531470.1:c.403T>G XP_011529772.1:p.Ser135Ala
XM_017030078.2:c.637T>G XP_016885567.1:p.Ser213Ala
NM_004654.4:c.637T>G MANE Select NP_004645.2:p.Ser213Ala
Search 100 bp 5'
Search 100 bp 3'