Canonical Allele Identifier: CA345736946

Gene: RNASEH1

Linked Data

• MyVariant Identifiers: chr2:g.3596683G>T (hg19) ; chr2:g.3549093G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.3549093G>T , CM000664.2:g.3549093G>T	GRCh38
NC_000002.11:g.3596683G>T , CM000664.1:g.3596683G>T	GRCh37
NC_000002.10:g.3574558G>T	NCBI36
NG_051310.1:g.14279C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315212.4:c.529C>A MANE Select	ENSP00000313350.3:p.Pro177Thr
ENST00000654051.1:c.529C>A	ENSP00000499604.1:p.Pro177Thr
ENST00000658393.1:c.529C>A	ENSP00000499330.1:p.Pro177Thr
ENST00000315212.3:c.529C>A	ENSP00000313350.3:p.Pro177Thr
ENST00000436842.5:c.*635C>A	ENSP00000404926.1:n.*635C>A
NM_001286834.1:c.451C>A	NP_001273763.1:p.Pro151Thr
NM_001286837.1:c.178C>A	NP_001273766.1:p.Pro60Thr
NM_002936.4:c.529C>A	NP_002927.2:p.Pro177Thr
XR_244873.1:n.636C>A
XR_922665.1:n.636C>A
XR_922666.1:n.636C>A
XR_922667.1:n.636C>A
XR_922668.1:n.636C>A
XR_922669.1:n.636C>A
XR_922670.1:n.636C>A
XR_922671.1:n.636C>A
XR_922672.1:n.636C>A
XR_922673.1:n.636C>A
XR_922674.1:n.636C>A
NM_001286834.2:c.451C>A	NP_001273763.1:p.Pro151Thr
NM_001286837.2:c.178C>A	NP_001273766.1:p.Pro60Thr
NM_002936.5:c.529C>A	NP_002927.2:p.Pro177Thr
NR_148532.1:n.640C>A
NR_148533.1:n.640C>A
NR_148534.1:n.640C>A
NM_001286837.3:c.178C>A	NP_001273766.1:p.Pro60Thr
NR_148532.2:n.602C>A
NR_148533.2:n.602C>A
NR_148534.2:n.602C>A
NM_001286834.3:c.451C>A	NP_001273763.1:p.Pro151Thr
NM_001378271.1:c.529C>A	NP_001365200.1:p.Pro177Thr
NM_001378272.1:c.526C>A	NP_001365201.1:p.Pro176Thr
NM_001378273.1:c.514C>A	NP_001365202.1:p.Pro172Thr
NM_002936.6:c.529C>A MANE Select	NP_002927.2:p.Pro177Thr
NR_165465.1:n.486C>A
NR_165466.1:n.583-12C>A
NR_165467.1:n.771C>A
NR_165468.1:n.574C>A