Canonical Allele Identifier: CA1500800364
Gene: HHIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144728808_144728811delinsGTTC , CM000666.2:g.144728808_144728811delinsGTTC GRCh38
NC_000004.11:g.145649960_145649963delinsGTTC , CM000666.1:g.145649960_145649963delinsGTTC GRCh37
NC_000004.10:g.145869410_145869413delinsGTTC NCBI36
NG_011496.1:g.87788_87791delinsGTTC

Transcript Alleles

HGVS Amino-acid change
ENST00000296575.8:c.1761-5933_1761-5930delinsGTTC MANE Select ENSP00000296575.3:n.1761-5933_1761-5930de...
ENST00000649263.1:c.328-312833_328-312830delinsGAAC ENSP00000497507.1:n.328-312833_328-312830...
ENST00000296575.7:c.1761-5933_1761-5930delinsGTTC ENSP00000296575.3:n.1761-5933_1761-5930de...
NM_022475.2:c.1761-5933_1761-5930delinsGTTC NP_071920.1:n.1761-5933_1761-5930delinsGT...
XM_005263178.3:c.1761-5933_1761-5930delinsGTTC XP_005263235.1:n.1761-5933_1761-5930delin...
XM_006714288.2:c.1761-5933_1761-5930delinsGTTC XP_006714351.1:n.1761-5933_1761-5930delin...
XM_005263178.5:c.1761-5933_1761-5930delinsGTTC XP_005263235.1:n.1761-5933_1761-5930delin...
XM_006714288.4:c.1761-5933_1761-5930delinsGTTC XP_006714351.1:n.1761-5933_1761-5930delin...
NM_022475.3:c.1761-5933_1761-5930delinsGTTC MANE Select NP_071920.1:n.1761-5933_1761-5930delinsGT...