Canonical Allele Identifier: CA917593
Gene: USP33 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.77722040T>C , CM000663.2:g.77722040T>C GRCh38
NC_000001.10:g.78187725T>C , CM000663.1:g.78187725T>C GRCh37
NC_000001.9:g.77960313T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_201624.3:c.1546A>G MANE Select NP_963918.1:p.Met516Val
ENST00000370794.7:c.1546A>G MANE Select ENSP00000359830.3:p.Met516Val
NM_001377430.1:c.1639A>G NP_001364359.1:p.Met547Val
NM_001377431.1:c.1546A>G NP_001364360.1:p.Met516Val
NM_001377432.1:c.1639A>G NP_001364361.1:p.Met547Val
NM_001377433.1:c.1639A>G NP_001364362.1:p.Met547Val
NM_001377434.1:c.1546A>G NP_001364363.1:p.Met516Val
NM_001377435.1:c.1546A>G NP_001364364.1:p.Met516Val
NM_001377436.1:c.1546A>G NP_001364365.1:p.Met516Val
NM_001377437.1:c.1546A>G NP_001364366.1:p.Met516Val
NM_001377438.1:c.1102A>G NP_001364367.1:p.Met368Val
NM_001377439.1:c.1102A>G NP_001364368.1:p.Met368Val
NM_015017.4:c.1639A>G NP_055832.3:p.Met547Val
NM_015017.5:c.1639A>G NP_055832.3:p.Met547Val
NM_201624.2:c.1546A>G NP_963918.1:p.Met516Val
NM_201626.2:c.1639A>G NP_963920.1:p.Met547Val
NM_201626.3:c.1639A>G NP_963920.1:p.Met547Val
ENST00000357428.5:c.1639A>G ENSP00000350009.1:p.Met547Val
ENST00000370792.7:c.1639A>G ENSP00000359828.3:p.Met547Val
ENST00000370793.5:c.1639A>G ENSP00000359829.1:p.Met547Val
ENST00000461986.5:n.360A>G
ENST00000481579.5:c.453A>G
XM_005270648.1:c.1639A>G XP_005270705.1:p.Met547Val
XM_005270649.1:c.1639A>G XP_005270706.1:p.Met547Val
XM_011541055.1:c.1639A>G XP_011539357.1:p.Met547Val
XM_011541056.1:c.1639A>G XP_011539358.1:p.Met547Val
XM_011541056.2:c.1639A>G XP_011539358.1:p.Met547Val
XM_017000722.2:c.1546A>G XP_016856211.1:p.Met516Val
XM_017000723.2:c.1546A>G XP_016856212.1:p.Met516Val
XM_017000724.2:c.1546A>G XP_016856213.1:p.Met516Val
XM_017000725.2:c.1546A>G XP_016856214.1:p.Met516Val
XM_017000726.2:c.1546A>G XP_016856215.1:p.Met516Val
XM_017000727.2:c.1102A>G XP_016856216.1:p.Met368Val
XM_017000728.2:c.1102A>G XP_016856217.1:p.Met368Val
XM_017000729.1:c.1639A>G XP_016856218.1:p.Met547Val
XR_946588.1:n.1662A>G
XR_946589.1:n.1662A>G