Canonical Allele Identifier: CA730337
Gene: ZCCHC17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.31346654G>A , CM000663.2:g.31346654G>A GRCh38
NC_000001.10:g.31819501G>A , CM000663.1:g.31819501G>A GRCh37
NC_000001.9:g.31592088G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_016505.4:c.332G>A MANE Select NP_057589.2:p.Arg111Gln
ENST00000344147.10:c.332G>A MANE Select ENSP00000343557.5:p.Arg111Gln
NM_001282566.1:c.398G>A NP_001269495.1:p.Arg133Gln
NM_001282566.2:c.398G>A NP_001269495.1:p.Arg133Gln
NM_001282567.1:c.260G>A NP_001269496.1:p.Arg87Gln
NM_001282567.2:c.260G>A NP_001269496.1:p.Arg87Gln
NM_001282568.1:c.332G>A NP_001269497.1:p.Arg111Gln
NM_001282568.2:c.332G>A NP_001269497.1:p.Arg111Gln
NM_001282569.1:c.308G>A NP_001269498.1:p.Arg103Gln
NM_001282569.2:c.308G>A NP_001269498.1:p.Arg103Gln
NM_001282570.1:c.260G>A NP_001269499.1:p.Arg87Gln
NM_001282570.2:c.260G>A NP_001269499.1:p.Arg87Gln
NM_001282571.1:c.146G>A NP_001269500.1:p.Arg49Gln
NM_001282571.2:c.146G>A NP_001269500.1:p.Arg49Gln
NM_001282572.1:c.317+7606G>A NP_001269501.1:n.317+7606G>A
NM_001282572.2:c.317+7606G>A NP_001269501.1:n.317+7606G>A
NM_001282573.1:c.293+7606G>A NP_001269502.1:n.293+7606G>A
NM_001282573.2:c.293+7606G>A NP_001269502.1:n.293+7606G>A
NM_001282574.1:c.332G>A NP_001269503.1:p.Arg111Gln
NM_001282574.2:c.332G>A NP_001269503.1:p.Arg111Gln
NM_016505.3:c.332G>A NP_057589.2:p.Arg111Gln
ENST00000344147.9:c.332G>A ENSP00000343557.5:p.Arg111Gln
ENST00000373714.5:c.332G>A ENSP00000362819.1:p.Arg111Gln
ENST00000422613.6:c.245G>A ENSP00000391336.3:p.Arg82Gln
ENST00000479629.5:n.535G>A
ENST00000546109.5:c.308G>A ENSP00000444742.1:p.Arg103Gln
ENST00000615916.4:c.398G>A ENSP00000480986.1:p.Arg133Gln
ENST00000616393.4:c.146G>A ENSP00000482122.1:p.Arg49Gln
ENST00000616859.4:c.293+7606G>A ENSP00000481743.1:n.293+7606G>A
ENST00000618216.4:c.332G>A ENSP00000481299.1:p.Arg111Gln
ENST00000627541.1:c.260G>A ENSP00000486079.1:p.Arg87Gln
XM_006710681.2:c.308G>A XP_006710744.1:p.Arg103Gln
XM_006710681.4:c.308G>A XP_006710744.1:p.Arg103Gln
XM_011541567.1:c.332G>A XP_011539869.1:p.Arg111Gln