Canonical Allele Identifier: CA9627715
Community Standard Title: NM_006969.5(ZNF28):c.1844C>T (p.Thr615Ile)
Gene: ZNF28 HGNC NCBI
ZNF600 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.52800001G>A , CM000681.2:g.52800001G>A GRCh38
NC_000019.9:g.53303254G>A , CM000681.1:g.53303254G>A GRCh37
NC_000019.8:g.57995066G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_006969.5:c.1844C>T (ZNF28) MANE Select NP_008900.3:p.Thr615Ile
ENST00000457749.7:c.1844C>T (ZNF28) MANE Select ENSP00000397693.2:p.Thr615Ile
NM_001369761.1:c.*1572C>T (ZNF28) NP_001356690.1:n.*1572C>T
NM_001369762.1:c.1685C>T (ZNF28) NP_001356691.1:p.Thr562Ile
NM_001369763.1:c.1835C>T (ZNF28) NP_001356692.1:p.Thr612Ile
NM_001369764.1:c.1802C>T (ZNF28) NP_001356693.1:p.Thr601Ile
NM_001369765.1:c.1736C>T (ZNF28) NP_001356694.1:p.Thr579Ile
NM_001369766.1:c.*1572C>T (ZNF28) NP_001356695.1:n.*1572C>T
NM_006969.3:c.1844C>T (ZNF28) NP_008900.3:p.Thr615Ile
NM_006969.4:c.1844C>T (ZNF28) NP_008900.3:p.Thr615Ile
NR_036599.1:n.2119C>T (ZNF28)
NR_036600.1:n.1874C>T (ZNF28)
NR_163139.1:n.2330C>T (ZNF28)
ENST00000360272.5:c.709-203C>T (ZNF600) ENSP00000353410.5:n.709-203C>T
ENST00000438150.2:c.1685C>T (ZNF28) ENSP00000412143.2:p.Thr562Ile
ENST00000457749.6:c.1844C>T (ZNF28) ENSP00000397693.2:p.Thr615Ile
XM_006723058.2:c.64-25300C>T (ZNF600) XP_006723121.1:n.64-25300C>T
XM_006723354.2:c.1802C>T (ZNF28) XP_006723417.1:p.Thr601Ile
XM_006723354.3:c.1802C>T (ZNF28) XP_006723417.1:p.Thr601Ile
XM_006723356.2:c.1592C>T (ZNF28) XP_006723419.1:p.Thr531Ile
XM_011527262.1:c.1844C>T (ZNF28) XP_011525564.1:p.Thr615Ile
XM_011527262.2:c.1844C>T (ZNF28) XP_011525564.1:p.Thr615Ile
XM_011527263.1:c.1508C>T (ZNF28) XP_011525565.1:p.Thr503Ile
XM_024451686.1:c.1508C>T (ZNF28) XP_024307454.1:p.Thr503Ile
XM_024451687.1:c.1685C>T (ZNF28) XP_024307455.1:p.Thr562Ile
XM_024451688.1:c.1685C>T (ZNF28) XP_024307456.1:p.Thr562Ile