Canonical Allele Identifier: CA1234605929
Gene: RNASEH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.3549091_3549092delinsAG , CM000664.2:g.3549091_3549092delinsAG GRCh38
NC_000002.11:g.3596681_3596682delinsAG , CM000664.1:g.3596681_3596682delinsAG GRCh37
NC_000002.10:g.3574556_3574557delinsAG NCBI36
NG_051310.1:g.14280_14281delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000315212.4:c.530_531delinsCT MANE Select ENSP00000313350.3:p.Pro177=
ENST00000654051.1:c.530_531delinsCT ENSP00000499604.1:p.Pro177=
ENST00000658393.1:c.530_531delinsCT ENSP00000499330.1:p.Pro177=
ENST00000315212.3:c.530_531delinsCT ENSP00000313350.3:p.Pro177=
ENST00000436842.5:c.*636_*637delinsCT ENSP00000404926.1:n.*636_*637delinsCT
NM_001286834.1:c.452_453delinsCT NP_001273763.1:p.Pro151=
NM_001286837.1:c.179_180delinsCT NP_001273766.1:p.Pro60=
NM_002936.4:c.530_531delinsCT NP_002927.2:p.Pro177=
XR_244873.1:n.637_638delinsCT
XR_922665.1:n.637_638delinsCT
XR_922666.1:n.637_638delinsCT
XR_922667.1:n.637_638delinsCT
XR_922668.1:n.637_638delinsCT
XR_922669.1:n.637_638delinsCT
XR_922670.1:n.637_638delinsCT
XR_922671.1:n.637_638delinsCT
XR_922672.1:n.637_638delinsCT
XR_922673.1:n.637_638delinsCT
XR_922674.1:n.637_638delinsCT
NM_001286834.2:c.452_453delinsCT NP_001273763.1:p.Pro151=
NM_001286837.2:c.179_180delinsCT NP_001273766.1:p.Pro60=
NM_002936.5:c.530_531delinsCT NP_002927.2:p.Pro177=
NR_148532.1:n.641_642delinsCT
NR_148533.1:n.641_642delinsCT
NR_148534.1:n.641_642delinsCT
NM_001286837.3:c.179_180delinsCT NP_001273766.1:p.Pro60=
NR_148532.2:n.603_604delinsCT
NR_148533.2:n.603_604delinsCT
NR_148534.2:n.603_604delinsCT
NM_001286834.3:c.452_453delinsCT NP_001273763.1:p.Pro151=
NM_001378271.1:c.530_531delinsCT NP_001365200.1:p.Pro177=
NM_001378272.1:c.527_528delinsCT NP_001365201.1:p.Pro176=
NM_001378273.1:c.515_516delinsCT NP_001365202.1:p.Pro172=
NM_002936.6:c.530_531delinsCT MANE Select NP_002927.2:p.Pro177=
NR_165465.1:n.487_488delinsCT
NR_165466.1:n.583-11_583-10delinsCT
NR_165467.1:n.772_773delinsCT
NR_165468.1:n.575_576delinsCT