Canonical Allele Identifier: CA1729070704
Gene: ZKSCAN5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99521178C>A , CM000669.2:g.99521178C>A GRCh38
NC_000007.13:g.99118801C>A , CM000669.1:g.99118801C>A GRCh37
NC_000007.12:g.98956737C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000326775.10:c.772+874C>A MANE Select ENSP00000322872.5:n.772+874C>A
ENST00000326775.9:c.772+874C>A ENSP00000322872.5:n.772+874C>A
ENST00000394170.6:c.772+874C>A ENSP00000377725.2:n.772+874C>A
ENST00000451158.5:c.772+874C>A ENSP00000392104.1:n.772+874C>A
ENST00000454175.1:c.636+1269C>A ENSP00000405716.1:n.636+1269C>A
NM_014569.3:c.772+874C>A NP_055384.1:n.772+874C>A
NM_145102.2:c.772+874C>A NP_659570.1:n.772+874C>A
XM_005250242.2:c.554-4635C>A XP_005250299.1:n.554-4635C>A
XM_005250243.2:c.-21+1269C>A XP_005250300.1:n.-21+1269C>A
XM_006715913.2:c.772+874C>A XP_006715976.1:n.772+874C>A
XM_011515999.1:c.325+874C>A XP_011514301.1:n.325+874C>A
NM_001318082.1:c.772+874C>A NP_001305011.1:n.772+874C>A
NM_001318083.1:c.554-4635C>A NP_001305012.1:n.554-4635C>A
NM_001318084.1:c.-21+1269C>A NP_001305013.1:n.-21+1269C>A
NM_145102.3:c.772+874C>A NP_659570.1:n.772+874C>A
XM_011515999.2:c.325+874C>A XP_011514301.1:n.325+874C>A
XM_017011921.2:c.769+874C>A XP_016867410.1:n.769+874C>A
XM_017011922.1:c.769+874C>A XP_016867411.1:n.769+874C>A
XM_017011924.1:c.554-4635C>A XP_016867413.1:n.554-4635C>A
XM_017011925.1:c.322+874C>A XP_016867414.1:n.322+874C>A
NM_001318082.2:c.772+874C>A NP_001305011.1:n.772+874C>A
NM_001318083.2:c.554-4635C>A NP_001305012.1:n.554-4635C>A
NM_014569.4:c.772+874C>A NP_055384.1:n.772+874C>A
NM_145102.4:c.772+874C>A MANE Select NP_659570.1:n.772+874C>A