Canonical Allele Identifier: CA2323583800

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12813164C= , CM000681.2:g.12813164C= GRCh38
NC_000019.9:g.12923978C= , CM000681.1:g.12923978C= GRCh37
NC_000019.8:g.12784978C= NCBI36
NG_012662.1:g.11551C= , LRG_278:g.11551C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221486.6:c.719C= (RNASEH2A) MANE Select ENSP00000221486.4:p.Thr240=
ENST00000593017.2:n.1005C= (RNASEH2A)
ENST00000639767.2:c.*598C= (THSD8) ENSP00000491410.2:n.*598C=
ENST00000643757.1:n.754C= (RNASEH2A)
ENST00000646769.1:c.*379C= (RNASEH2A) ENSP00000495175.1:n.*379C=
ENST00000221486.4:c.719C= (RNASEH2A) ENSP00000221486.3:p.Thr240=
ENST00000589765.1:n.41+12014G= (HOOK2)
ENST00000593017.1:n.1134C= (RNASEH2A)
NM_006397.2:c.719C= , LRG_278t1:c.719C= (RNASEH2A) NP_006388.2:p.Thr240=
XM_006722619.2:c.587C= (RNASEH2A) XP_006722682.1:p.Thr196=
NM_006397.3:c.719C= (RNASEH2A) MANE Select NP_006388.2:p.Thr240=