Canonical Allele Identifier: CA8637981

Gene: ZNF652

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49312652G>C , CM000679.2:g.49312652G>C	GRCh38
NC_000017.10:g.47390014G>C , CM000679.1:g.47390014G>C	GRCh37
NC_000017.9:g.44745013G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430262.3:c.1048+46C>G MANE Select	ENSP00000416305.2:n.1048+46C>G
ENST00000362063.6:c.1048+46C>G	ENSP00000354686.2:n.1048+46C>G
ENST00000430262.2:c.1048+46C>G	ENSP00000416305.2:n.1048+46C>G
ENST00000508237.5:c.508+46C>G	ENSP00000424848.1:n.508+46C>G
NM_001145365.1:c.1048+46C>G	NP_001138837.1:n.1048+46C>G
NM_014897.2:c.1048+46C>G	NP_055712.1:n.1048+46C>G
XM_005257166.1:c.508+46C>G	XP_005257223.1:n.508+46C>G
XR_934423.1:n.1259+46C>G
XR_934424.1:n.890+46C>G
NR_135579.1:n.1096+46C>G
XM_024450653.1:c.1048+46C>G	XP_024306421.1:n.1048+46C>G
XM_024450654.1:c.1048+46C>G	XP_024306422.1:n.1048+46C>G
XM_024450655.1:c.1048+46C>G	XP_024306423.1:n.1048+46C>G
XM_024450656.1:c.508+46C>G	XP_024306424.1:n.508+46C>G
XR_934423.2:n.1460+46C>G
NM_001145365.2:c.1048+46C>G	NP_001138837.1:n.1048+46C>G
NR_135579.2:n.1232+46C>G
NM_001145365.3:c.1048+46C>G MANE Select	NP_001138837.1:n.1048+46C>G