Canonical Allele Identifier: CA414981971
Gene: USP9Y HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.14838707C>G (hg19) chrY:g.12726774C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12726774C>G , CM000686.2:g.12726774C>G GRCh38
NC_000024.9:g.14838707C>G , CM000686.1:g.14838707C>G GRCh37
NC_000024.8:g.13348101C>G NCBI36
NG_008311.1:g.30548C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.638C>G ENSP00000498372.1:p.Ser213Ter
ENST00000338981.7:c.638C>G MANE Select ENSP00000342812.3:p.Ser213Ter
ENST00000426564.6:n.650C>G
NM_004654.3:c.638C>G NP_004645.2:p.Ser213Ter
XM_011531469.1:c.638C>G XP_011529771.1:p.Ser213Ter
XM_011531470.1:c.404C>G XP_011529772.1:p.Ser135Ter
XM_017030078.2:c.638C>G XP_016885567.1:p.Ser213Ter
NM_004654.4:c.638C>G MANE Select NP_004645.2:p.Ser213Ter
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