Canonical Allele Identifier: CA2799183483

Gene: RNASEH2B

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.50943380_50943386del , CM000675.2:g.50943380_50943386del	GRCh38
NC_000013.10:g.51517516_51517522del , CM000675.1:g.51517516_51517522del	GRCh37
NC_000013.9:g.50415517_50415523del	NCBI36
NG_009055.1:g.38625_38631del , LRG_279:g.38625_38631del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336617.8:c.496_502del MANE Select	ENSP00000337623.2:p.Trp166LysfsTer11
ENST00000422660.6:c.496_502del	ENSP00000389877.1:p.Trp166LysfsTer11
ENST00000459681.3:n.179_185del
ENST00000495244.7:n.507_513del
ENST00000611510.5:c.406_412del	ENSP00000481236.3:p.Trp136LysfsTer11
ENST00000616907.2:c.496_502del	ENSP00000482701.2:p.Trp166LysfsTer11
ENST00000642207.1:c.235_241del
ENST00000642454.1:c.406_412del	ENSP00000494221.1:p.Trp136LysfsTer11
ENST00000642721.1:c.496_502del	ENSP00000495650.1:p.Trp166LysfsTer11
ENST00000642995.1:c.379_385del	ENSP00000493499.1:p.Trp127LysfsTer11
ENST00000643159.1:c.406_412del	ENSP00000495587.1:p.Trp136LysfsTer11
ENST00000643215.1:c.366_372del
ENST00000643405.1:c.144_150del
ENST00000643529.1:c.9_15del
ENST00000643682.1:c.496_502del	ENSP00000493655.1:p.Trp166LysfsTer11
ENST00000643774.1:c.460_466del	ENSP00000495482.1:p.Trp154LysfsTer11
ENST00000644034.1:c.65-4607_65-4601del	ENSP00000495456.1:n.65-4607_65-4601del
ENST00000644183.1:c.386_392del	ENSP00000495657.1:n.386_392del
ENST00000644297.1:c.*354_*360del	ENSP00000495519.1:n.*354_*360del
ENST00000644420.1:n.522_528del
ENST00000644425.1:c.447_453del
ENST00000644518.1:c.*363_*369del	ENSP00000495793.1:n.*363_*369del
ENST00000645188.1:c.487_493del	ENSP00000496224.1:p.Trp163LysfsTer11
ENST00000645333.1:n.428_434del
ENST00000645370.1:c.331_337del	ENSP00000494019.1:p.Trp111LysfsTer11
ENST00000645618.1:c.406_412del	ENSP00000495429.1:p.Trp136LysfsTer11
ENST00000645712.1:n.520_526del
ENST00000645955.1:c.496_502del	ENSP00000495755.1:p.Trp166LysfsTer11
ENST00000645990.1:c.496_502del	ENSP00000496571.1:p.Trp166LysfsTer11
ENST00000646092.1:c.460_466del	ENSP00000496293.1:p.Trp154LysfsTer11
ENST00000646279.1:n.793_799del
ENST00000646339.1:c.158_164del	ENSP00000495773.1:n.158_164del
ENST00000646709.1:c.406_412del	ENSP00000495278.1:p.Trp136LysfsTer11
ENST00000646731.1:c.487_493del	ENSP00000493828.1:p.Trp163LysfsTer11
ENST00000646960.1:c.496_502del	ENSP00000496481.1:p.Trp166LysfsTer11
ENST00000646964.1:n.1135_1141del
ENST00000647387.1:c.406_412del	ENSP00000495487.1:p.Trp136LysfsTer11
ENST00000336617.7:c.496_502del	ENSP00000337623.2:p.Trp166LysfsTer11
ENST00000422660.5:c.496_502del	ENSP00000389877.1:p.Trp166LysfsTer11
ENST00000495244.6:n.507_513del
ENST00000611510.4:c.496_502del	ENSP00000481236.2:p.Trp166LysfsTer11
ENST00000613449.4:n.2558_2564del
ENST00000621641.1:n.84_90del
NM_001142279.2:c.496_502del , LRG_279t1:c.496_502del	NP_001135751.1:p.Trp166LysfsTer11
NM_024570.3:c.496_502del , LRG_279t2:c.496_502del	NP_078846.2:p.Trp166LysfsTer11
XM_005266524.2:c.496_502del	XP_005266581.1:p.Trp166LysfsTer11
XM_005266525.2:c.496_502del	XP_005266582.1:p.Trp166LysfsTer11
XM_006719867.2:c.478_484del	XP_006719930.1:p.Trp160LysfsTer11
XM_011535229.1:c.496_502del	XP_011533531.1:p.Trp166LysfsTer11
XM_011535230.1:c.496_502del	XP_011533532.1:p.Trp166LysfsTer11
XM_011535231.1:c.496_502del	XP_011533533.1:p.Trp166LysfsTer11
XM_011535232.1:c.334_340del	XP_011533534.1:p.Trp112LysfsTer11
XM_011535233.1:c.88_94del	XP_011533535.1:p.Trp30LysfsTer11
XM_011535234.1:c.496_502del	XP_011533536.1:p.Trp166LysfsTer?
XM_006719867.4:c.478_484del	XP_006719930.1:p.Trp160LysfsTer11
XM_011535230.2:c.496_502del	XP_011533532.1:p.Trp166LysfsTer11
XM_011535231.2:c.496_502del	XP_011533533.1:p.Trp166LysfsTer11
XM_011535233.2:c.88_94del	XP_011533535.1:p.Trp30LysfsTer11
XM_017020747.1:c.496_502del	XP_016876236.1:p.Trp166LysfsTer11
NM_024570.4:c.496_502del MANE Select	NP_078846.2:p.Trp166LysfsTer11