Canonical Allele Identifier: CA3233680865

Gene: RNASEH2A THSD8 HOOK2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12807213G= , CM000681.2:g.12807213G=	GRCh38
NC_000019.9:g.12918027G= , CM000681.1:g.12918027G=	GRCh37
NC_000019.8:g.12779027G=	NCBI36
NG_012662.1:g.5600G= , LRG_278:g.5600G=

Transcript Alleles

HGVS	Amino-acid Change
NM_006397.3:c.207G= (RNASEH2A) MANE Select	NP_006388.2:p.Lys69=
ENST00000221486.6:c.207G= (RNASEH2A) MANE Select	ENSP00000221486.4:p.Lys69=
NM_006397.2:c.207G= , LRG_278t1:c.207G= (RNASEH2A)	NP_006388.2:p.Lys69=
ENST00000221486.4:c.207G= (RNASEH2A)	ENSP00000221486.3:p.Lys69=
ENST00000589765.1:n.41+17965C= (HOOK2)
ENST00000590121.1:n.204G= (RNASEH2A)
ENST00000590121.2:c.204G= (RNASEH2A)	ENSP00000495087.1:p.Lys68=
ENST00000590279.1:n.404G= (RNASEH2A)
ENST00000590279.2:n.622G= (RNASEH2A)
ENST00000593017.1:n.622G= (RNASEH2A)
ENST00000593017.2:n.404G= (RNASEH2A)
ENST00000639767.2:c.*86G= (THSD8)	ENSP00000491410.2:n.*86G=
ENST00000643757.1:n.242G= (RNASEH2A)
ENST00000646769.1:c.199+134G= (RNASEH2A)	ENSP00000495175.1:n.199+134G=
XM_006722619.2:c.75G= (RNASEH2A)	XP_006722682.1:p.Lys25=