Canonical Allele Identifier: CA394695067

Gene: USP7

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.8894627A>G , CM000678.2:g.8894627A>G	GRCh38
NC_000016.9:g.8988484A>G , CM000678.1:g.8988484A>G	GRCh37
NC_000016.8:g.8895985A>G	NCBI36
NG_046847.1:g.73858T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_003470.3:c.3125T>C MANE Select	NP_003461.2:p.Ile1042Thr
ENST00000344836.9:c.3125T>C MANE Select	ENSP00000343535.4:p.Ile1042Thr
NM_001286457.1:c.3077T>C	NP_001273386.1:p.Ile1026Thr
NM_001286457.2:c.3077T>C	NP_001273386.2:p.Ile1026Thr
NM_001286458.1:c.2828T>C	NP_001273387.1:p.Ile943Thr
NM_001286458.2:c.2828T>C	NP_001273387.1:p.Ile943Thr
NM_001321858.1:c.2951T>C	NP_001308787.1:p.Ile984Thr
NM_001321858.2:c.2951T>C	NP_001308787.1:p.Ile984Thr
NM_003470.2:c.3125T>C	NP_003461.2:p.Ile1042Thr
NR_135826.1:n.3106T>C
NR_135826.2:n.3106T>C
ENST00000344836.8:c.3125T>C	ENSP00000343535.4:p.Ile1042Thr
ENST00000381886.8:c.3077T>C	ENSP00000371310.4:p.Ile1026Thr
ENST00000563961.5:c.*2710T>C	ENSP00000454362.1:n.*2710T>C
ENST00000565455.5:c.*3108T>C	ENSP00000456258.1:n.*3108T>C
ENST00000673704.1:c.3230T>C	ENSP00000501290.1:p.Ile1077Thr
XM_017023652.1:c.3125T>C	XP_016879141.1:p.Ile1042Thr
XM_017023653.2:c.3077T>C	XP_016879142.1:p.Ile1026Thr