Canonical Allele Identifier: CA7857516

Gene: ZSCAN10

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3090344C>T , CM000678.2:g.3090344C>T	GRCh38
NC_000016.9:g.3140345C>T , CM000678.1:g.3140345C>T	GRCh37
NC_000016.8:g.3080346C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576985.6:c.1090G>A MANE Select	ENSP00000458879.2:p.Ala364Thr
ENST00000252463.6:c.925G>A	ENSP00000252463.2:p.Ala309Thr
ENST00000538082.5:c.679G>A	ENSP00000440047.2:p.Ala227Thr
ENST00000571903.5:n.1614G>A
ENST00000572431.1:c.-93G>A	ENSP00000460473.1:n.-93G>A
ENST00000575108.5:c.-93G>A	ENSP00000459520.1:n.-93G>A
ENST00000576985.5:c.1090G>A	ENSP00000458879.2:p.Ala364Thr
NM_001282415.1:c.-93G>A	NP_001269344.1:n.-93G>A
NM_001282416.1:c.679G>A	NP_001269345.1:p.Ala227Thr
NM_032805.2:c.1090G>A	NP_116194.2:p.Ala364Thr
NM_001365272.1:c.544G>A	NP_001352201.1:p.Ala182Thr
NM_001365273.1:c.-93G>A	NP_001352202.1:n.-93G>A
XM_017023791.1:c.1090G>A	XP_016879280.1:p.Ala364Thr
XM_017023792.1:c.994G>A	XP_016879281.1:p.Ala332Thr
NM_032805.3:c.1090G>A MANE Select	NP_116194.2:p.Ala364Thr
NM_001282415.2:c.-93G>A	NP_001269344.1:n.-93G>A
NM_001282416.2:c.679G>A	NP_001269345.1:p.Ala227Thr