Canonical Allele Identifier: CA337718119

Gene: USP9Y TTTY15

Linked Data

• dbSNP Id: rs753935491
• gnomAD v3: Y-12663260-G-C
• gnomAD v4: Y-12663260-G-C
• MyVariant Identifiers: chrY:g.14775191G>C (hg19) ; chrY:g.12663260G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12663260G>C , CM000686.2:g.12663260G>C	GRCh38
NC_000024.9:g.14775191G>C , CM000686.1:g.14775191G>C	GRCh37
NC_000024.8:g.13284585G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000417071.1:n.170+554G>C
ENST00000440408.5:n.373+554G>C
ENST00000457658.6:n.1004+554G>C (USP9Y)
ENST00000651177.1:c.-248+554G>C (USP9Y)	ENSP00000498372.1:n.-248+554G>C
NR_001545.2:n.340+554G>C (TTTY15)
XR_938612.1:n.490+44C>G
XR_938613.1:n.433+101C>G
XR_002958838.1:n.660+44C>G
XR_002958839.1:n.603+101C>G
NR_001545.3:n.355+554G>C (TTTY15)
NR_174085.1:n.355+554G>C (TTTY15)
NR_174086.1:n.355+554G>C (TTTY15)
NR_174087.1:n.355+554G>C (TTTY15)
NR_174088.1:n.355+554G>C (TTTY15)