Canonical Allele Identifier: CA1500800341
Gene: HHIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144728777_144728778delinsTG , CM000666.2:g.144728777_144728778delinsTG GRCh38
NC_000004.11:g.145649929_145649930delinsTG , CM000666.1:g.145649929_145649930delinsTG GRCh37
NC_000004.10:g.145869379_145869380delinsTG NCBI36
NG_011496.1:g.87757_87758delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000296575.8:c.1761-5964_1761-5963delinsTG MANE Select ENSP00000296575.3:n.1761-5964_1761-5963de...
ENST00000649263.1:c.328-312800_328-312799delinsCA ENSP00000497507.1:n.328-312800_328-312799...
ENST00000296575.7:c.1761-5964_1761-5963delinsTG ENSP00000296575.3:n.1761-5964_1761-5963de...
NM_022475.2:c.1761-5964_1761-5963delinsTG NP_071920.1:n.1761-5964_1761-5963delinsTG...
XM_005263178.3:c.1761-5964_1761-5963delinsTG XP_005263235.1:n.1761-5964_1761-5963delin...
XM_006714288.2:c.1761-5964_1761-5963delinsTG XP_006714351.1:n.1761-5964_1761-5963delin...
XM_005263178.5:c.1761-5964_1761-5963delinsTG XP_005263235.1:n.1761-5964_1761-5963delin...
XM_006714288.4:c.1761-5964_1761-5963delinsTG XP_006714351.1:n.1761-5964_1761-5963delin...
NM_022475.3:c.1761-5964_1761-5963delinsTG MANE Select NP_071920.1:n.1761-5964_1761-5963delinsTG...