Canonical Allele Identifier: CA380110393
Gene: HIPK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.33286625C>T , CM000673.2:g.33286625C>T GRCh38
NC_000011.9:g.33308171C>T , CM000673.1:g.33308171C>T GRCh37
NC_000011.8:g.33264747C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_005734.5:c.211C>T MANE Select NP_005725.3:p.Pro71Ser
ENST00000303296.9:c.211C>T MANE Select ENSP00000304226.4:p.Pro71Ser
NM_001048200.2:c.211C>T NP_001041665.1:p.Pro71Ser
NM_001048200.3:c.211C>T NP_001041665.1:p.Pro71Ser
NM_001278162.1:c.211C>T NP_001265091.1:p.Pro71Ser
NM_001278162.2:c.211C>T NP_001265091.1:p.Pro71Ser
NM_001278163.1:c.211C>T NP_001265092.1:p.Pro71Ser
NM_001278163.2:c.211C>T NP_001265092.1:p.Pro71Ser
NM_005734.4:c.211C>T NP_005725.3:p.Pro71Ser
ENST00000303296.8:c.211C>T ENSP00000304226.4:p.Pro71Ser
ENST00000379016.7:c.211C>T ENSP00000368301.3:p.Pro71Ser
ENST00000456517.2:c.211C>T ENSP00000398241.1:p.Pro71Ser
ENST00000525975.5:c.211C>T ENSP00000431710.1:p.Pro71Ser
ENST00000531504.5:c.211C>T ENSP00000433594.1:p.Pro71Ser
XM_005252729.2:c.211C>T XP_005252786.1:p.Pro71Ser
XM_005252729.3:c.211C>T XP_005252786.1:p.Pro71Ser
XM_011519835.1:c.211C>T XP_011518137.1:p.Pro71Ser
XM_017017076.1:c.211C>T XP_016872565.1:p.Pro71Ser