Canonical Allele Identifier: CA519891476
Gene: USP9Y HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.14922684T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12810749T>C , CM000686.2:g.12810749T>C GRCh38
NC_000024.9:g.14922684T>C , CM000686.1:g.14922684T>C GRCh37
NC_000024.8:g.13432078T>C NCBI36
NG_008311.1:g.114525T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.4170T>C ENSP00000498372.1:p.Asn1390=
ENST00000338981.7:c.4170T>C MANE Select ENSP00000342812.3:p.Asn1390=
ENST00000426564.6:n.4182T>C
NM_004654.3:c.4170T>C NP_004645.2:p.Asn1390=
XM_011531469.1:c.4170T>C XP_011529771.1:p.Asn1390=
XM_011531470.1:c.3936T>C XP_011529772.1:p.Asn1312=
XM_017030078.2:c.4185T>C XP_016885567.1:p.Asn1395=
NM_004654.4:c.4170T>C MANE Select NP_004645.2:p.Asn1390=