Canonical Allele Identifier: CA394477587

Gene: ZSCAN10

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3089551T>C , CM000678.2:g.3089551T>C	GRCh38
NC_000016.9:g.3139552T>C , CM000678.1:g.3139552T>C	GRCh37
NC_000016.8:g.3079553T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_032805.3:c.1883A>G MANE Select	NP_116194.2:p.His628Arg
ENST00000576985.6:c.1883A>G MANE Select	ENSP00000458879.2:p.His628Arg
NM_001282415.1:c.701A>G	NP_001269344.1:p.His234Arg
NM_001282415.2:c.701A>G	NP_001269344.1:p.His234Arg
NM_001282416.1:c.1472A>G	NP_001269345.1:p.His491Arg
NM_001282416.2:c.1472A>G	NP_001269345.1:p.His491Arg
NM_001365272.1:c.1337A>G	NP_001352201.1:p.His446Arg
NM_001365273.1:c.701A>G	NP_001352202.1:p.His234Arg
NM_032805.2:c.1883A>G	NP_116194.2:p.His628Arg
ENST00000252463.6:c.1718A>G	ENSP00000252463.2:p.His573Arg
ENST00000538082.5:c.1472A>G	ENSP00000440047.2:p.His491Arg
ENST00000575108.5:c.701A>G	ENSP00000459520.1:p.His234Arg
ENST00000576985.5:c.1883A>G	ENSP00000458879.2:p.His628Arg
XM_017023791.1:c.1883A>G	XP_016879280.1:p.His628Arg
XM_017023792.1:c.1787A>G	XP_016879281.1:p.His596Arg