Canonical Allele Identifier: CA2323583792

Gene: RNASEH2A THSD8 HOOK2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12813149G= , CM000681.2:g.12813149G=	GRCh38
NC_000019.9:g.12923963G= , CM000681.1:g.12923963G=	GRCh37
NC_000019.8:g.12784963G=	NCBI36
NG_012662.1:g.11536G= , LRG_278:g.11536G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221486.6:c.704G= (RNASEH2A) MANE Select	ENSP00000221486.4:p.Arg235=
ENST00000593017.2:n.990G= (RNASEH2A)
ENST00000639767.2:c.*583G= (THSD8)	ENSP00000491410.2:n.*583G=
ENST00000643757.1:n.739G= (RNASEH2A)
ENST00000646769.1:c.*364G= (RNASEH2A)	ENSP00000495175.1:n.*364G=
ENST00000221486.4:c.704G= (RNASEH2A)	ENSP00000221486.3:p.Arg235=
ENST00000589765.1:n.41+12029C= (HOOK2)
ENST00000593017.1:n.1119G= (RNASEH2A)
NM_006397.2:c.704G= , LRG_278t1:c.704G= (RNASEH2A)	NP_006388.2:p.Arg235=
XM_006722619.2:c.572G= (RNASEH2A)	XP_006722682.1:p.Arg191=
NM_006397.3:c.704G= (RNASEH2A) MANE Select	NP_006388.2:p.Arg235=