Canonical Allele Identifier: CA415007401

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14889951A>C (hg19) ; chrY:g.12778017A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12778017A>C , CM000686.2:g.12778017A>C	GRCh38
NC_000024.9:g.14889951A>C , CM000686.1:g.14889951A>C	GRCh37
NC_000024.8:g.13399345A>C	NCBI36
NG_008311.1:g.81792A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.2640-2A>C	ENSP00000498372.1:n.2640-2A>C
ENST00000338981.7:c.2640-2A>C MANE Select	ENSP00000342812.3:n.2640-2A>C
ENST00000426564.6:n.2652-2A>C
NM_004654.3:c.2640-2A>C	NP_004645.2:n.2640-2A>C
XM_011531469.1:c.2640-2A>C	XP_011529771.1:n.2640-2A>C
XM_011531470.1:c.2406-2A>C	XP_011529772.1:n.2406-2A>C
XM_017030078.2:c.2655-2A>C	XP_016885567.1:n.2655-2A>C
NM_004654.4:c.2640-2A>C MANE Select	NP_004645.2:n.2640-2A>C