Canonical Allele Identifier: CA12906321

Gene: ZNF704

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.80798602G>A , CM000670.2:g.80798602G>A	GRCh38
NC_000008.10:g.81710837G>A , CM000670.1:g.81710837G>A	GRCh37
NC_000008.9:g.81873392G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519936.2:c.743+22772C>T	ENSP00000427715.2:n.743+22772C>T
ENST00000327835.7:c.221+22772C>T MANE Select	ENSP00000331462.3:n.221+22772C>T
ENST00000519936.1:c.221+22772C>T	ENSP00000427715.1:n.221+22772C>T
ENST00000520336.1:n.148+15510C>T
NM_001033723.2:c.221+22772C>T	NP_001028895.1:n.221+22772C>T
XM_005251279.3:c.743+22772C>T	XP_005251336.2:n.743+22772C>T
XM_006716464.2:c.221+22772C>T	XP_006716527.1:n.221+22772C>T
XR_928797.1:n.878+22772C>T
XM_005251279.4:c.743+22772C>T	XP_005251336.2:n.743+22772C>T
XM_017013725.1:c.245+22772C>T	XP_016869214.1:n.245+22772C>T
XR_928797.2:n.1084+22772C>T
NM_001033723.3:c.221+22772C>T MANE Select	NP_001028895.1:n.221+22772C>T
NM_001367783.1:c.743+22772C>T	NP_001354712.1:n.743+22772C>T