Canonical Allele Identifier: CA7857830

Gene: ZSCAN10

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3092762C>T , CM000678.2:g.3092762C>T	GRCh38
NC_000016.9:g.3142763C>T , CM000678.1:g.3142763C>T	GRCh37
NC_000016.8:g.3082764C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576985.6:c.176G>A MANE Select	ENSP00000458879.2:p.Arg59Gln
ENST00000252463.6:c.11G>A	ENSP00000252463.2:p.Arg4Gln
ENST00000538082.5:c.33G>A	ENSP00000440047.2:p.Thr11=
ENST00000571903.5:n.475G>A
ENST00000572431.1:c.-518-934G>A	ENSP00000460473.1:n.-518-934G>A
ENST00000572548.1:c.176G>A	ENSP00000461871.2:p.Arg59Gln
ENST00000575108.5:c.-786-446G>A	ENSP00000459520.1:n.-786-446G>A
ENST00000576483.1:c.176G>A	ENSP00000458260.2:p.Arg59Gln
ENST00000576985.5:c.176G>A	ENSP00000458879.2:p.Arg59Gln
ENST00000577059.1:n.324G>A
NM_001282415.1:c.-786-446G>A	NP_001269344.1:n.-786-446G>A
NM_001282416.1:c.33G>A	NP_001269345.1:p.Thr11=
NM_032805.2:c.176G>A	NP_116194.2:p.Arg59Gln
NM_001365272.1:c.33G>A	NP_001352201.1:p.Thr11=
NM_001365273.1:c.-518-934G>A	NP_001352202.1:n.-518-934G>A
XM_017023791.1:c.176G>A	XP_016879280.1:p.Arg59Gln
XM_017023792.1:c.176G>A	XP_016879281.1:p.Arg59Gln
NM_032805.3:c.176G>A MANE Select	NP_116194.2:p.Arg59Gln
NM_001282415.2:c.-786-446G>A	NP_001269344.1:n.-786-446G>A
NM_001282416.2:c.33G>A	NP_001269345.1:p.Thr11=