Canonical Allele Identifier: CA9913186

Gene: ZFP64

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.52152684T>G , CM000682.2:g.52152684T>G	GRCh38
NC_000020.10:g.50769223T>G , CM000682.1:g.50769223T>G	GRCh37
NC_000020.9:g.50202630T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216923.5:c.1508A>C MANE Select	ENSP00000216923.4:p.His503Pro
ENST00000216923.4:c.1508A>C	ENSP00000216923.4:p.His503Pro
ENST00000346617.8:c.1346A>C	ENSP00000344615.4:p.His449Pro
ENST00000361387.6:c.763+7439A>C	ENSP00000355179.2:n.763+7439A>C
ENST00000371515.8:c.1502A>C	ENSP00000360570.4:p.His501Pro
ENST00000371518.6:c.763+7439A>C	ENSP00000360573.2:n.763+7439A>C
ENST00000477786.5:n.588+7439A>C
NM_018197.2:c.1508A>C	NP_060667.2:p.His503Pro
NM_022088.4:c.1346A>C	NP_071371.3:p.His449Pro
NM_199426.1:c.1502A>C	NP_955458.1:p.His501Pro
NM_199427.2:c.763+7439A>C	NP_955459.2:n.763+7439A>C
XM_005260449.1:c.1034A>C	XP_005260506.1:p.His345Pro
XM_011528900.1:c.1034A>C	XP_011527202.1:p.His345Pro
XM_011528900.2:c.1034A>C	XP_011527202.1:p.His345Pro
XM_017027945.2:c.757+7439A>C	XP_016883434.1:n.757+7439A>C
XM_017027946.2:c.1340A>C	XP_016883435.1:p.His447Pro
XM_017027947.2:c.601+7439A>C	XP_016883436.1:n.601+7439A>C
XM_017027948.2:c.1034A>C	XP_016883437.1:p.His345Pro
XM_017027949.1:c.1034A>C	XP_016883438.1:p.His345Pro
NM_018197.3:c.1508A>C MANE Select	NP_060667.2:p.His503Pro
NM_022088.5:c.1346A>C	NP_071371.3:p.His449Pro
NM_199426.2:c.1502A>C	NP_955458.1:p.His501Pro
NM_199427.3:c.763+7439A>C	NP_955459.2:n.763+7439A>C