Canonical Allele Identifier: CA1729149511
Gene: ZSCAN25 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99642511C= , CM000669.2:g.99642511C= GRCh38
NC_000007.13:g.99240134C= , CM000669.1:g.99240134C= GRCh37
NC_000007.12:g.99078070C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011515909.1:c.805+18331C= XP_011514211.1:n.805+18331C=
XM_011515910.1:c.806-4960C= XP_011514212.1:n.806-4960C=
XR_927402.1:n.1466+18331C=
NM_001350984.1:c.805+18331C= NP_001337913.1:n.805+18331C=
NM_001350985.1:c.805+18331C= NP_001337914.1:n.805+18331C=
XM_011515909.2:c.805+18331C= XP_011514211.1:n.805+18331C=
XM_011515910.2:c.806-4960C= XP_011514212.1:n.806-4960C=
XR_927402.2:n.1465+18331C=
NM_001350984.2:c.805+18331C= NP_001337913.1:n.805+18331C=
NM_001350985.2:c.805+18331C= NP_001337914.1:n.805+18331C=