Canonical Allele Identifier: CA2323583937

Gene: RNASEH2A THSD8 HOOK2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12813438G= , CM000681.2:g.12813438G=	GRCh38
NC_000019.9:g.12924252G= , CM000681.1:g.12924252G=	GRCh37
NC_000019.8:g.12785252G=	NCBI36
NG_012662.1:g.11825G= , LRG_278:g.11825G=

Transcript Alleles

HGVS	Amino-acid Change
NM_006397.3:c.872G= (RNASEH2A) MANE Select	NP_006388.2:p.Arg291=
ENST00000221486.6:c.872G= (RNASEH2A) MANE Select	ENSP00000221486.4:p.Arg291=
NM_006397.2:c.872G= , LRG_278t1:c.872G= (RNASEH2A)	NP_006388.2:p.Arg291=
ENST00000221486.4:c.872G= (RNASEH2A)	ENSP00000221486.3:p.Arg291=
ENST00000589765.1:n.41+11740C= (HOOK2)
ENST00000593017.1:n.1287G= (RNASEH2A)
ENST00000593017.2:n.1158G= (RNASEH2A)
ENST00000639767.2:c.*751G= (THSD8)	ENSP00000491410.2:n.*751G=
ENST00000643757.1:n.907G= (RNASEH2A)
XM_006722619.2:c.740G= (RNASEH2A)	XP_006722682.1:p.Arg247=