Canonical Allele Identifier: CA1234605817
Gene: RNASEH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.3548880_3548900delinsTATTTGAAATAAGTTTTTAGA , CM000664.2:g.3548880_3548900delinsTATTTGAAATAAGTTTTTAGA GRCh38
NC_000002.11:g.3596470_3596490delinsTATTTGAAATAAGTTTTTAGA , CM000664.1:g.3596470_3596490delinsTATTTGAAATAAGTTTTTAGA GRCh37
NC_000002.10:g.3574345_3574365delinsTATTTGAAATAAGTTTTTAGA NCBI36
NG_051310.1:g.14472_14492delinsTCTAAAAACTTATTTCAAATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000315212.4:c.564+158_565-156delinsTCTAAAAACTTATTTCAAATA MANE Select ENSP00000313350.3:n.564+158_565-156delinsTCTAAAAACTTATTTCAAAT...
ENST00000654051.1:c.564+158_565-156delinsTCTAAAAACTTATTTCAAATA ENSP00000499604.1:n.564+158_565-156delinsTCTAAAAACTTATTTCAAAT...
ENST00000658393.1:c.564+158_565-156delinsTCTAAAAACTTATTTCAAATA ENSP00000499330.1:n.564+158_565-156delinsTCTAAAAACTTATTTCAAAT...
ENST00000315212.3:c.564+158_565-156delinsTCTAAAAACTTATTTCAAATA ENSP00000313350.3:n.564+158_565-156delinsTCTAAAAACTTATTTCAAAT...
ENST00000436842.5:c.*670+158_*671-156delinsTCTAAAAACTTATTTCAAATA ENSP00000404926.1:n.*670+158_*671-156delinsTCTAAAAACTTATTTCAA...
NM_001286834.1:c.486+158_487-156delinsTCTAAAAACTTATTTCAAATA NP_001273763.1:n.486+158_487-156delinsTCTAAAAACTTATTTCAAATA
NM_001286837.1:c.213+158_214-156delinsTCTAAAAACTTATTTCAAATA NP_001273766.1:n.213+158_214-156delinsTCTAAAAACTTATTTCAAATA
NM_002936.4:c.564+158_565-156delinsTCTAAAAACTTATTTCAAATA NP_002927.2:n.564+158_565-156delinsTCTAAAAACTTATTTCAAATA
XR_244873.1:n.671+158_672-160delinsTCTAAAAACTTATTTCAAATA
XR_922665.1:n.671+158_672-156delinsTCTAAAAACTTATTTCAAATA
XR_922666.1:n.671+158_672-156delinsTCTAAAAACTTATTTCAAATA
XR_922667.1:n.671+158_672-156delinsTCTAAAAACTTATTTCAAATA
XR_922668.1:n.671+158_672-156delinsTCTAAAAACTTATTTCAAATA
XR_922669.1:n.671+158_672-156delinsTCTAAAAACTTATTTCAAATA
XR_922670.1:n.671+158_672-156delinsTCTAAAAACTTATTTCAAATA
XR_922671.1:n.671+158_672-156delinsTCTAAAAACTTATTTCAAATA
XR_922672.1:n.671+158_672-156delinsTCTAAAAACTTATTTCAAATA
XR_922673.1:n.671+158_672-156delinsTCTAAAAACTTATTTCAAATA
XR_922674.1:n.671+158_672-156delinsTCTAAAAACTTATTTCAAATA
NM_001286834.2:c.486+158_487-156delinsTCTAAAAACTTATTTCAAATA NP_001273763.1:n.486+158_487-156delinsTCTAAAAACTTATTTCAAATA
NM_001286837.2:c.213+158_214-156delinsTCTAAAAACTTATTTCAAATA NP_001273766.1:n.213+158_214-156delinsTCTAAAAACTTATTTCAAATA
NM_002936.5:c.564+158_565-156delinsTCTAAAAACTTATTTCAAATA NP_002927.2:n.564+158_565-156delinsTCTAAAAACTTATTTCAAATA
NR_148532.1:n.675+158_676-156delinsTCTAAAAACTTATTTCAAATA
NR_148533.1:n.675+158_676-160delinsTCTAAAAACTTATTTCAAATA
NR_148534.1:n.675+158_676-156delinsTCTAAAAACTTATTTCAAATA
NM_001286837.3:c.213+158_214-156delinsTCTAAAAACTTATTTCAAATA NP_001273766.1:n.213+158_214-156delinsTCTAAAAACTTATTTCAAATA
NR_148532.2:n.637+158_638-156delinsTCTAAAAACTTATTTCAAATA
NR_148533.2:n.637+158_638-160delinsTCTAAAAACTTATTTCAAATA
NR_148534.2:n.637+158_638-156delinsTCTAAAAACTTATTTCAAATA
NM_001286834.3:c.486+158_487-156delinsTCTAAAAACTTATTTCAAATA NP_001273763.1:n.486+158_487-156delinsTCTAAAAACTTATTTCAAATA
NM_001378271.1:c.564+158_565-156delinsTCTAAAAACTTATTTCAAATA NP_001365200.1:n.564+158_565-156delinsTCTAAAAACTTATTTCAAATA
NM_001378272.1:c.561+158_562-156delinsTCTAAAAACTTATTTCAAATA NP_001365201.1:n.561+158_562-156delinsTCTAAAAACTTATTTCAAATA
NM_001378273.1:c.549+158_550-156delinsTCTAAAAACTTATTTCAAATA NP_001365202.1:n.549+158_550-156delinsTCTAAAAACTTATTTCAAATA
NM_002936.6:c.564+158_565-156delinsTCTAAAAACTTATTTCAAATA MANE Select NP_002927.2:n.564+158_565-156delinsTCTAAAAACTTATTTCAAATA
NR_165465.1:n.521+158_522-156delinsTCTAAAAACTTATTTCAAATA
NR_165466.1:n.606+158_607-156delinsTCTAAAAACTTATTTCAAATA
NR_165467.1:n.806+158_807-156delinsTCTAAAAACTTATTTCAAATA
NR_165468.1:n.609+158_610-156delinsTCTAAAAACTTATTTCAAATA