Canonical Allele Identifier: CA1234605878
Gene: RNASEH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.3548986A= , CM000664.2:g.3548986A= GRCh38
NC_000002.11:g.3596576A= , CM000664.1:g.3596576A= GRCh37
NC_000002.10:g.3574451A= NCBI36
NG_051310.1:g.14386T=

Transcript Alleles

HGVS Amino-acid change
ENST00000315212.4:c.564+72T= MANE Select ENSP00000313350.3:n.564+72T=
ENST00000654051.1:c.564+72T= ENSP00000499604.1:n.564+72T=
ENST00000658393.1:c.564+72T= ENSP00000499330.1:n.564+72T=
ENST00000315212.3:c.564+72T= ENSP00000313350.3:n.564+72T=
ENST00000436842.5:c.*670+72T= ENSP00000404926.1:n.*670+72T=
NM_001286834.1:c.486+72T= NP_001273763.1:n.486+72T=
NM_001286837.1:c.213+72T= NP_001273766.1:n.213+72T=
NM_002936.4:c.564+72T= NP_002927.2:n.564+72T=
XR_244873.1:n.671+72T=
XR_922665.1:n.671+72T=
XR_922666.1:n.671+72T=
XR_922667.1:n.671+72T=
XR_922668.1:n.671+72T=
XR_922669.1:n.671+72T=
XR_922670.1:n.671+72T=
XR_922671.1:n.671+72T=
XR_922672.1:n.671+72T=
XR_922673.1:n.671+72T=
XR_922674.1:n.671+72T=
NM_001286834.2:c.486+72T= NP_001273763.1:n.486+72T=
NM_001286837.2:c.213+72T= NP_001273766.1:n.213+72T=
NM_002936.5:c.564+72T= NP_002927.2:n.564+72T=
NR_148532.1:n.675+72T=
NR_148533.1:n.675+72T=
NR_148534.1:n.675+72T=
NM_001286837.3:c.213+72T= NP_001273766.1:n.213+72T=
NR_148532.2:n.637+72T=
NR_148533.2:n.637+72T=
NR_148534.2:n.637+72T=
NM_001286834.3:c.486+72T= NP_001273763.1:n.486+72T=
NM_001378271.1:c.564+72T= NP_001365200.1:n.564+72T=
NM_001378272.1:c.561+72T= NP_001365201.1:n.561+72T=
NM_001378273.1:c.549+72T= NP_001365202.1:n.549+72T=
NM_002936.6:c.564+72T= MANE Select NP_002927.2:n.564+72T=
NR_165465.1:n.521+72T=
NR_165466.1:n.606+72T=
NR_165467.1:n.806+72T=
NR_165468.1:n.609+72T=