Canonical Allele Identifier: CA1729149584

Gene: ZSCAN25

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99642549C= , CM000669.2:g.99642549C=	GRCh38
NC_000007.13:g.99240172C= , CM000669.1:g.99240172C=	GRCh37
NC_000007.12:g.99078108C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_011515909.1:c.805+18369C=	XP_011514211.1:n.805+18369C=
XM_011515910.1:c.806-4922C=	XP_011514212.1:n.806-4922C=
XR_927402.1:n.1466+18369C=
NM_001350984.1:c.805+18369C=	NP_001337913.1:n.805+18369C=
NM_001350985.1:c.805+18369C=	NP_001337914.1:n.805+18369C=
XM_011515909.2:c.805+18369C=	XP_011514211.1:n.805+18369C=
XM_011515910.2:c.806-4922C=	XP_011514212.1:n.806-4922C=
XR_927402.2:n.1465+18369C=
NM_001350984.2:c.805+18369C=	NP_001337913.1:n.805+18369C=
NM_001350985.2:c.805+18369C=	NP_001337914.1:n.805+18369C=