Canonical Allele Identifier: CA1234605833

Gene: RNASEH1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.3548910_3548911delinsCA , CM000664.2:g.3548910_3548911delinsCA	GRCh38
NC_000002.11:g.3596500_3596501delinsCA , CM000664.1:g.3596500_3596501delinsCA	GRCh37
NC_000002.10:g.3574375_3574376delinsCA	NCBI36
NG_051310.1:g.14461_14462delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315212.4:c.564+147_564+148delinsTG MANE Select	ENSP00000313350.3:n.564+147_564+148delinsTG
ENST00000654051.1:c.564+147_564+148delinsTG	ENSP00000499604.1:n.564+147_564+148delinsTG
ENST00000658393.1:c.564+147_564+148delinsTG	ENSP00000499330.1:n.564+147_564+148delinsTG
ENST00000315212.3:c.564+147_564+148delinsTG	ENSP00000313350.3:n.564+147_564+148delinsTG
ENST00000436842.5:c.*670+147_*670+148delinsTG	ENSP00000404926.1:n.*670+147_*670+148delinsTG
NM_001286834.1:c.486+147_486+148delinsTG	NP_001273763.1:n.486+147_486+148delinsTG
NM_001286837.1:c.213+147_213+148delinsTG	NP_001273766.1:n.213+147_213+148delinsTG
NM_002936.4:c.564+147_564+148delinsTG	NP_002927.2:n.564+147_564+148delinsTG
XR_244873.1:n.671+147_671+148delinsTG
XR_922665.1:n.671+147_671+148delinsTG
XR_922666.1:n.671+147_671+148delinsTG
XR_922667.1:n.671+147_671+148delinsTG
XR_922668.1:n.671+147_671+148delinsTG
XR_922669.1:n.671+147_671+148delinsTG
XR_922670.1:n.671+147_671+148delinsTG
XR_922671.1:n.671+147_671+148delinsTG
XR_922672.1:n.671+147_671+148delinsTG
XR_922673.1:n.671+147_671+148delinsTG
XR_922674.1:n.671+147_671+148delinsTG
NM_001286834.2:c.486+147_486+148delinsTG	NP_001273763.1:n.486+147_486+148delinsTG
NM_001286837.2:c.213+147_213+148delinsTG	NP_001273766.1:n.213+147_213+148delinsTG
NM_002936.5:c.564+147_564+148delinsTG	NP_002927.2:n.564+147_564+148delinsTG
NR_148532.1:n.675+147_675+148delinsTG
NR_148533.1:n.675+147_675+148delinsTG
NR_148534.1:n.675+147_675+148delinsTG
NM_001286837.3:c.213+147_213+148delinsTG	NP_001273766.1:n.213+147_213+148delinsTG
NR_148532.2:n.637+147_637+148delinsTG
NR_148533.2:n.637+147_637+148delinsTG
NR_148534.2:n.637+147_637+148delinsTG
NM_001286834.3:c.486+147_486+148delinsTG	NP_001273763.1:n.486+147_486+148delinsTG
NM_001378271.1:c.564+147_564+148delinsTG	NP_001365200.1:n.564+147_564+148delinsTG
NM_001378272.1:c.561+147_561+148delinsTG	NP_001365201.1:n.561+147_561+148delinsTG
NM_001378273.1:c.549+147_549+148delinsTG	NP_001365202.1:n.549+147_549+148delinsTG
NM_002936.6:c.564+147_564+148delinsTG MANE Select	NP_002927.2:n.564+147_564+148delinsTG
NR_165465.1:n.521+147_521+148delinsTG
NR_165466.1:n.606+147_606+148delinsTG
NR_165467.1:n.806+147_806+148delinsTG
NR_165468.1:n.609+147_609+148delinsTG