Canonical Allele Identifier: CA2323580958

Gene: RNASEH2A THSD8 HOOK2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12807328C= , CM000681.2:g.12807328C=	GRCh38
NC_000019.9:g.12918142C= , CM000681.1:g.12918142C=	GRCh37
NC_000019.8:g.12779142C=	NCBI36
NG_012662.1:g.5715C= , LRG_278:g.5715C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221486.6:c.322C= (RNASEH2A) MANE Select	ENSP00000221486.4:p.Arg108=
ENST00000590121.2:c.319C= (RNASEH2A)	ENSP00000495087.1:p.Arg107=
ENST00000590279.2:n.737C= (RNASEH2A)
ENST00000593017.2:n.519C= (RNASEH2A)
ENST00000639767.2:c.*201C= (THSD8)	ENSP00000491410.2:n.*201C=
ENST00000643757.1:n.357C= (RNASEH2A)
ENST00000646769.1:c.200-91C= (RNASEH2A)	ENSP00000495175.1:n.200-91C=
ENST00000221486.4:c.322C= (RNASEH2A)	ENSP00000221486.3:p.Arg108=
ENST00000589765.1:n.41+17850G= (HOOK2)
ENST00000590121.1:n.319C= (RNASEH2A)
ENST00000590279.1:n.519C= (RNASEH2A)
ENST00000593017.1:n.737C= (RNASEH2A)
NM_006397.2:c.322C= , LRG_278t1:c.322C= (RNASEH2A)	NP_006388.2:p.Arg108=
XM_006722619.2:c.190C= (RNASEH2A)	XP_006722682.1:p.Arg64=
NM_006397.3:c.322C= (RNASEH2A) MANE Select	NP_006388.2:p.Arg108=