Canonical Allele Identifier: CA1234605916

Gene: RNASEH1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.3549058A= , CM000664.2:g.3549058A=	GRCh38
NC_000002.11:g.3596648A= , CM000664.1:g.3596648A=	GRCh37
NC_000002.10:g.3574523A=	NCBI36
NG_051310.1:g.14314T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315212.4:c.564T= MANE Select	ENSP00000313350.3:p.His188=
ENST00000654051.1:c.564T=	ENSP00000499604.1:p.His188=
ENST00000658393.1:c.564T=	ENSP00000499330.1:p.His188=
ENST00000315212.3:c.564T=	ENSP00000313350.3:p.His188=
ENST00000436842.5:c.*670T=	ENSP00000404926.1:n.*670T=
NM_001286834.1:c.486T=	NP_001273763.1:p.His162=
NM_001286837.1:c.213T=	NP_001273766.1:p.His71=
NM_002936.4:c.564T=	NP_002927.2:p.His188=
XR_244873.1:n.671T=
XR_922665.1:n.671T=
XR_922666.1:n.671T=
XR_922667.1:n.671T=
XR_922668.1:n.671T=
XR_922669.1:n.671T=
XR_922670.1:n.671T=
XR_922671.1:n.671T=
XR_922672.1:n.671T=
XR_922673.1:n.671T=
XR_922674.1:n.671T=
NM_001286834.2:c.486T=	NP_001273763.1:p.His162=
NM_001286837.2:c.213T=	NP_001273766.1:p.His71=
NM_002936.5:c.564T=	NP_002927.2:p.His188=
NR_148532.1:n.675T=
NR_148533.1:n.675T=
NR_148534.1:n.675T=
NM_001286837.3:c.213T=	NP_001273766.1:p.His71=
NR_148532.2:n.637T=
NR_148533.2:n.637T=
NR_148534.2:n.637T=
NM_001286834.3:c.486T=	NP_001273763.1:p.His162=
NM_001378271.1:c.564T=	NP_001365200.1:p.His188=
NM_001378272.1:c.561T=	NP_001365201.1:p.His187=
NM_001378273.1:c.549T=	NP_001365202.1:p.His183=
NM_002936.6:c.564T= MANE Select	NP_002927.2:p.His188=
NR_165465.1:n.521T=
NR_165466.1:n.606T=
NR_165467.1:n.806T=
NR_165468.1:n.609T=