Canonical Allele Identifier: CA414989197
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12810681A>G , CM000686.2:g.12810681A>G GRCh38
NC_000024.9:g.14922616A>G , CM000686.1:g.14922616A>G GRCh37
NC_000024.8:g.13432010A>G NCBI36
NG_008311.1:g.114457A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.4102A>G ENSP00000498372.1:p.Arg1368Gly
ENST00000338981.7:c.4102A>G MANE Select ENSP00000342812.3:p.Arg1368Gly
ENST00000426564.6:n.4114A>G
NM_004654.3:c.4102A>G NP_004645.2:p.Arg1368Gly
XM_011531469.1:c.4102A>G XP_011529771.1:p.Arg1368Gly
XM_011531470.1:c.3868A>G XP_011529772.1:p.Arg1290Gly
XM_017030078.2:c.4117A>G XP_016885567.1:p.Arg1373Gly
NM_004654.4:c.4102A>G MANE Select NP_004645.2:p.Arg1368Gly