Canonical Allele Identifier: CA1729149579
Gene: ZSCAN25 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99642541G= , CM000669.2:g.99642541G= GRCh38
NC_000007.13:g.99240164G= , CM000669.1:g.99240164G= GRCh37
NC_000007.12:g.99078100G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011515909.1:c.805+18361G= XP_011514211.1:n.805+18361G=
XM_011515910.1:c.806-4930G= XP_011514212.1:n.806-4930G=
XR_927402.1:n.1466+18361G=
NM_001350984.1:c.805+18361G= NP_001337913.1:n.805+18361G=
NM_001350985.1:c.805+18361G= NP_001337914.1:n.805+18361G=
XM_011515909.2:c.805+18361G= XP_011514211.1:n.805+18361G=
XM_011515910.2:c.806-4930G= XP_011514212.1:n.806-4930G=
XR_927402.2:n.1465+18361G=
NM_001350984.2:c.805+18361G= NP_001337913.1:n.805+18361G=
NM_001350985.2:c.805+18361G= NP_001337914.1:n.805+18361G=