Canonical Allele Identifier: CA2202576598

Gene: ZSCAN10

Linked Data

• dbSNP Id: rs11644978
• gnomAD v4: 16-3092910-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3092910C>A , CM000678.2:g.3092910C>A	GRCh38
NC_000016.9:g.3142911C>A , CM000678.1:g.3142911C>A	GRCh37
NC_000016.8:g.3082912C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576985.6:c.28G>T MANE Select	ENSP00000458879.2:p.Val10Leu
ENST00000538082.5:c.-116G>T	ENSP00000440047.2:n.-116G>T
ENST00000571903.5:n.327G>T
ENST00000572431.1:c.-518-1082G>T	ENSP00000460473.1:n.-518-1082G>T
ENST00000572548.1:c.28G>T	ENSP00000461871.2:p.Val10Leu
ENST00000575108.5:c.-786-594G>T	ENSP00000459520.1:n.-786-594G>T
ENST00000576483.1:c.28G>T	ENSP00000458260.2:p.Val10Leu
ENST00000576985.5:c.28G>T	ENSP00000458879.2:p.Val10Leu
ENST00000577059.1:n.176G>T
NM_001282415.1:c.-786-594G>T	NP_001269344.1:n.-786-594G>T
NM_001282416.1:c.-116G>T	NP_001269345.1:n.-116G>T
NM_032805.2:c.28G>T	NP_116194.2:p.Val10Leu
NM_001365272.1:c.-116G>T	NP_001352201.1:n.-116G>T
NM_001365273.1:c.-518-1082G>T	NP_001352202.1:n.-518-1082G>T
XM_017023791.1:c.28G>T	XP_016879280.1:p.Val10Leu
XM_017023792.1:c.28G>T	XP_016879281.1:p.Val10Leu
NM_032805.3:c.28G>T MANE Select	NP_116194.2:p.Val10Leu
NM_001282415.2:c.-786-594G>T	NP_001269344.1:n.-786-594G>T
NM_001282416.2:c.-116G>T	NP_001269345.1:n.-116G>T