Canonical Allele Identifier: CA10573300
Gene: USP9Y HGNC NCBI

Linked Data

dbSNP Id: rs745519399
ExAC: Y:14922671 A / G
gnomAD v2: Y-14922671-A-G
gnomAD v3: Y-12810736-A-G
gnomAD v4: Y-12810736-A-G
MyVariant Identifiers: chrY:g.14922671A>G (hg19) chrY:g.12810736A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12810736A>G , CM000686.2:g.12810736A>G GRCh38
NC_000024.9:g.14922671A>G , CM000686.1:g.14922671A>G GRCh37
NC_000024.8:g.13432065A>G NCBI36
NG_008311.1:g.114512A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.4157A>G ENSP00000498372.1:p.Asn1386Ser
ENST00000338981.7:c.4157A>G MANE Select ENSP00000342812.3:p.Asn1386Ser
ENST00000426564.6:n.4169A>G
NM_004654.3:c.4157A>G NP_004645.2:p.Asn1386Ser
XM_011531469.1:c.4157A>G XP_011529771.1:p.Asn1386Ser
XM_011531470.1:c.3923A>G XP_011529772.1:p.Asn1308Ser
XM_017030078.2:c.4172A>G XP_016885567.1:p.Asn1391Ser
NM_004654.4:c.4157A>G MANE Select NP_004645.2:p.Asn1386Ser
Search 100 bp 5'
Search 100 bp 3'