Canonical Allele Identifier: CA414992775
Gene: USP9Y HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.14924952T>C (hg19) chrY:g.12813017T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12813017T>C , CM000686.2:g.12813017T>C GRCh38
NC_000024.9:g.14924952T>C , CM000686.1:g.14924952T>C GRCh37
NC_000024.8:g.13434346T>C NCBI36
NG_008311.1:g.116793T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.4574T>C ENSP00000498372.1:p.Leu1525Ser
ENST00000338981.7:c.4574T>C MANE Select ENSP00000342812.3:p.Leu1525Ser
ENST00000426564.6:n.4586T>C
NM_004654.3:c.4574T>C NP_004645.2:p.Leu1525Ser
XM_011531469.1:c.4574T>C XP_011529771.1:p.Leu1525Ser
XM_011531470.1:c.4340T>C XP_011529772.1:p.Leu1447Ser
XM_017030078.2:c.4589T>C XP_016885567.1:p.Leu1530Ser
NM_004654.4:c.4574T>C MANE Select NP_004645.2:p.Leu1525Ser
Search 100 bp 5'
Search 100 bp 3'