Canonical Allele Identifier: CA2323580655

Gene: RNASEH2A THSD8 HOOK2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12806790C= , CM000681.2:g.12806790C=	GRCh38
NC_000019.9:g.12917604C= , CM000681.1:g.12917604C=	GRCh37
NC_000019.8:g.12778604C=	NCBI36
NG_012662.1:g.5177C= , LRG_278:g.5177C=
NG_029901.1:g.91G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221486.6:c.117C= (RNASEH2A) MANE Select	ENSP00000221486.4:p.Gly39=
ENST00000590121.2:c.114C= (RNASEH2A)	ENSP00000495087.1:p.Gly38=
ENST00000590279.2:n.199C= (RNASEH2A)
ENST00000593017.2:n.107C= (RNASEH2A)
ENST00000639767.2:c.*7-218C= (THSD8)	ENSP00000491410.2:n.*7-218C=
ENST00000643364.1:n.801C= (THSD8)
ENST00000646769.1:c.117C= (RNASEH2A)	ENSP00000495175.1:p.Gly39=
ENST00000221486.4:c.117C= (RNASEH2A)	ENSP00000221486.3:p.Gly39=
ENST00000589765.1:n.41+18388G= (HOOK2)
ENST00000590121.1:n.114C= (RNASEH2A)
ENST00000590279.1:n.107C= (RNASEH2A)
ENST00000593017.1:n.199C= (RNASEH2A)
NM_006397.2:c.117C= , LRG_278t1:c.117C= (RNASEH2A)	NP_006388.2:p.Gly39=
XM_006722619.2:c.-5-218C= (RNASEH2A)	XP_006722682.1:n.-5-218C=
NM_006397.3:c.117C= (RNASEH2A) MANE Select	NP_006388.2:p.Gly39=