Canonical Allele Identifier: CA1234605926

Gene: RNASEH1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.3549087G= , CM000664.2:g.3549087G=	GRCh38
NC_000002.11:g.3596677G= , CM000664.1:g.3596677G=	GRCh37
NC_000002.10:g.3574552G=	NCBI36
NG_051310.1:g.14285C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315212.4:c.535C= MANE Select	ENSP00000313350.3:p.Arg179=
ENST00000654051.1:c.535C=	ENSP00000499604.1:p.Arg179=
ENST00000658393.1:c.535C=	ENSP00000499330.1:p.Arg179=
ENST00000315212.3:c.535C=	ENSP00000313350.3:p.Arg179=
ENST00000436842.5:c.*641C=	ENSP00000404926.1:n.*641C=
NM_001286834.1:c.457C=	NP_001273763.1:p.Arg153=
NM_001286837.1:c.184C=	NP_001273766.1:p.Arg62=
NM_002936.4:c.535C=	NP_002927.2:p.Arg179=
XR_244873.1:n.642C=
XR_922665.1:n.642C=
XR_922666.1:n.642C=
XR_922667.1:n.642C=
XR_922668.1:n.642C=
XR_922669.1:n.642C=
XR_922670.1:n.642C=
XR_922671.1:n.642C=
XR_922672.1:n.642C=
XR_922673.1:n.642C=
XR_922674.1:n.642C=
NM_001286834.2:c.457C=	NP_001273763.1:p.Arg153=
NM_001286837.2:c.184C=	NP_001273766.1:p.Arg62=
NM_002936.5:c.535C=	NP_002927.2:p.Arg179=
NR_148532.1:n.646C=
NR_148533.1:n.646C=
NR_148534.1:n.646C=
NM_001286837.3:c.184C=	NP_001273766.1:p.Arg62=
NR_148532.2:n.608C=
NR_148533.2:n.608C=
NR_148534.2:n.608C=
NM_001286834.3:c.457C=	NP_001273763.1:p.Arg153=
NM_001378271.1:c.535C=	NP_001365200.1:p.Arg179=
NM_001378272.1:c.532C=	NP_001365201.1:p.Arg178=
NM_001378273.1:c.520C=	NP_001365202.1:p.Arg174=
NM_002936.6:c.535C= MANE Select	NP_002927.2:p.Arg179=
NR_165465.1:n.492C=
NR_165466.1:n.583-6C=
NR_165467.1:n.777C=
NR_165468.1:n.580C=