Canonical Allele Identifier: CA2323582478

Gene: RNASEH2A THSD8 HOOK2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12810323C= , CM000681.2:g.12810323C=	GRCh38
NC_000019.9:g.12921137C= , CM000681.1:g.12921137C=	GRCh37
NC_000019.8:g.12782137C=	NCBI36
NG_012662.1:g.8710C= , LRG_278:g.8710C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221486.6:c.556C= (RNASEH2A) MANE Select	ENSP00000221486.4:p.Arg186=
ENST00000593017.2:n.842C= (RNASEH2A)
ENST00000639767.2:c.*435C= (THSD8)	ENSP00000491410.2:n.*435C=
ENST00000643757.1:n.591C= (RNASEH2A)
ENST00000646769.1:c.*216C= (RNASEH2A)	ENSP00000495175.1:n.*216C=
ENST00000221486.4:c.556C= (RNASEH2A)	ENSP00000221486.3:p.Arg186=
ENST00000589765.1:n.41+14855G= (HOOK2)
ENST00000593017.1:n.971C= (RNASEH2A)
NM_006397.2:c.556C= , LRG_278t1:c.556C= (RNASEH2A)	NP_006388.2:p.Arg186=
XM_006722619.2:c.424C= (RNASEH2A)	XP_006722682.1:p.Arg142=
NM_006397.3:c.556C= (RNASEH2A) MANE Select	NP_006388.2:p.Arg186=