Canonical Allele Identifier: CA2748668651

Gene: RNASEH1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.3549142_3549143insCACACCCAACAC , CM000664.2:g.3549142_3549143insCACACCCAACAC	GRCh38
NC_000002.11:g.3596732_3596733insCACACCCAACAC , CM000664.1:g.3596732_3596733insCACACCCAACAC	GRCh37
NC_000002.10:g.3574607_3574608insCACACCCAACAC	NCBI36
NG_051310.1:g.14229_14230insGTGTTGGGTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315212.4:c.510-31_510-30insGTGTTGGGTGTG MANE Select	ENSP00000313350.3:n.510-31_510-30insGTGTTGGGTGTG
ENST00000654051.1:c.510-31_510-30insGTGTTGGGTGTG	ENSP00000499604.1:n.510-31_510-30insGTGTTGGGTGTG
ENST00000658393.1:c.510-31_510-30insGTGTTGGGTGTG	ENSP00000499330.1:n.510-31_510-30insGTGTTGGGTGTG
ENST00000315212.3:c.510-31_510-30insGTGTTGGGTGTG	ENSP00000313350.3:n.510-31_510-30insGTGTTGGGTGTG
ENST00000436842.5:c.*616-31_*616-30insGTGTTGGGTGTG	ENSP00000404926.1:n.*616-31_*616-30insGTGTTGGGTGTG
NM_001286834.1:c.432-31_432-30insGTGTTGGGTGTG	NP_001273763.1:n.432-31_432-30insGTGTTGGGTGTG
NM_001286837.1:c.159-31_159-30insGTGTTGGGTGTG	NP_001273766.1:n.159-31_159-30insGTGTTGGGTGTG
NM_002936.4:c.510-31_510-30insGTGTTGGGTGTG	NP_002927.2:n.510-31_510-30insGTGTTGGGTGTG
XR_244873.1:n.617-31_617-30insGTGTTGGGTGTG
XR_922665.1:n.617-31_617-30insGTGTTGGGTGTG
XR_922666.1:n.617-31_617-30insGTGTTGGGTGTG
XR_922667.1:n.617-31_617-30insGTGTTGGGTGTG
XR_922668.1:n.617-31_617-30insGTGTTGGGTGTG
XR_922669.1:n.617-31_617-30insGTGTTGGGTGTG
XR_922670.1:n.617-31_617-30insGTGTTGGGTGTG
XR_922671.1:n.617-31_617-30insGTGTTGGGTGTG
XR_922672.1:n.617-31_617-30insGTGTTGGGTGTG
XR_922673.1:n.617-31_617-30insGTGTTGGGTGTG
XR_922674.1:n.617-31_617-30insGTGTTGGGTGTG
NM_001286834.2:c.432-31_432-30insGTGTTGGGTGTG	NP_001273763.1:n.432-31_432-30insGTGTTGGGTGTG
NM_001286837.2:c.159-31_159-30insGTGTTGGGTGTG	NP_001273766.1:n.159-31_159-30insGTGTTGGGTGTG
NM_002936.5:c.510-31_510-30insGTGTTGGGTGTG	NP_002927.2:n.510-31_510-30insGTGTTGGGTGTG
NR_148532.1:n.621-31_621-30insGTGTTGGGTGTG
NR_148533.1:n.621-31_621-30insGTGTTGGGTGTG
NR_148534.1:n.621-31_621-30insGTGTTGGGTGTG
NM_001286837.3:c.159-31_159-30insGTGTTGGGTGTG	NP_001273766.1:n.159-31_159-30insGTGTTGGGTGTG
NR_148532.2:n.583-31_583-30insGTGTTGGGTGTG
NR_148533.2:n.583-31_583-30insGTGTTGGGTGTG
NR_148534.2:n.583-31_583-30insGTGTTGGGTGTG
NM_001286834.3:c.432-31_432-30insGTGTTGGGTGTG	NP_001273763.1:n.432-31_432-30insGTGTTGGGTGTG
NM_001378271.1:c.510-31_510-30insGTGTTGGGTGTG	NP_001365200.1:n.510-31_510-30insGTGTTGGGTGTG
NM_001378272.1:c.507-31_507-30insGTGTTGGGTGTG	NP_001365201.1:n.507-31_507-30insGTGTTGGGTGTG
NM_001378273.1:c.510-46_510-45insGTGTTGGGTGTG	NP_001365202.1:n.510-46_510-45insGTGTTGGGTGTG
NM_002936.6:c.510-31_510-30insGTGTTGGGTGTG MANE Select	NP_002927.2:n.510-31_510-30insGTGTTGGGTGTG
NR_165465.1:n.467-31_467-30insGTGTTGGGTGTG
NR_165466.1:n.583-62_583-61insGTGTTGGGTGTG
NR_165467.1:n.752-31_752-30insGTGTTGGGTGTG
NR_165468.1:n.555-31_555-30insGTGTTGGGTGTG