Canonical Allele Identifier: CA10573390

Gene: USP9Y

Linked Data

• dbSNP Id: rs780956487
• ExAC: Y:14945826 G / T
• MyVariant Identifiers: chrY:g.14945826G>T (hg19) ; chrY:g.14945826_14945827delinsTT (hg19) ; chrY:g.12833900G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12833900G>T , CM000686.2:g.12833900G>T	GRCh38
NC_000024.9:g.14945826G>T , CM000686.1:g.14945826G>T	GRCh37
NC_000024.8:g.13455220G>T	NCBI36
NG_008311.1:g.137667G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.5195+39G>T	ENSP00000498372.1:n.5195+39G>T
ENST00000338981.7:c.5195+39G>T MANE Select	ENSP00000342812.3:n.5195+39G>T
ENST00000426564.6:n.5207+39G>T
NM_004654.3:c.5195+39G>T	NP_004645.2:n.5195+39G>T
XM_011531469.1:c.5195+39G>T	XP_011529771.1:n.5195+39G>T
XM_011531470.1:c.4961+39G>T	XP_011529772.1:n.4961+39G>T
XM_017030078.2:c.5210+39G>T	XP_016885567.1:n.5210+39G>T
NM_004654.4:c.5195+39G>T MANE Select	NP_004645.2:n.5195+39G>T