Canonical Allele Identifier: CA576410121

Gene: ZSCAN25

Linked Data

• gnomAD v2: 7-99240162-TAGTCACCCCCA-T
• MyVariant Identifiers: chr7:g.99240163_99240173del (hg19) ; chr7:g.99642540_99642550del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99642540_99642550del , CM000669.2:g.99642540_99642550del	GRCh38
NC_000007.13:g.99240163_99240173del , CM000669.1:g.99240163_99240173del	GRCh37
NC_000007.12:g.99078099_99078109del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_011515909.1:c.805+18360_805+18370del	XP_011514211.1:n.805+18360_805+18370del
XM_011515910.1:c.806-4931_806-4921del	XP_011514212.1:n.806-4931_806-4921del
XR_927402.1:n.1466+18360_1466+18370del
NM_001350984.1:c.805+18360_805+18370del	NP_001337913.1:n.805+18360_805+18370del
NM_001350985.1:c.805+18360_805+18370del	NP_001337914.1:n.805+18360_805+18370del
XM_011515909.2:c.805+18360_805+18370del	XP_011514211.1:n.805+18360_805+18370del
XM_011515910.2:c.806-4931_806-4921del	XP_011514212.1:n.806-4931_806-4921del
XR_927402.2:n.1465+18360_1465+18370del
NM_001350984.2:c.805+18360_805+18370del	NP_001337913.1:n.805+18360_805+18370del
NM_001350985.2:c.805+18360_805+18370del	NP_001337914.1:n.805+18360_805+18370del