Canonical Allele Identifier: CA1500800436
Gene: HHIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144728878_144728881delinsATTG , CM000666.2:g.144728878_144728881delinsATTG GRCh38
NC_000004.11:g.145650030_145650033delinsATTG , CM000666.1:g.145650030_145650033delinsATTG GRCh37
NC_000004.10:g.145869480_145869483delinsATTG NCBI36
NG_011496.1:g.87858_87861delinsATTG

Transcript Alleles

HGVS Amino-acid change
ENST00000296575.8:c.1761-5863_1761-5860delinsATTG MANE Select ENSP00000296575.3:n.1761-5863_1761-5860de...
ENST00000649263.1:c.328-312903_328-312900delinsCAAT ENSP00000497507.1:n.328-312903_328-312900...
ENST00000296575.7:c.1761-5863_1761-5860delinsATTG ENSP00000296575.3:n.1761-5863_1761-5860de...
NM_022475.2:c.1761-5863_1761-5860delinsATTG NP_071920.1:n.1761-5863_1761-5860delinsAT...
XM_005263178.3:c.1761-5863_1761-5860delinsATTG XP_005263235.1:n.1761-5863_1761-5860delin...
XM_006714288.2:c.1761-5863_1761-5860delinsATTG XP_006714351.1:n.1761-5863_1761-5860delin...
XM_005263178.5:c.1761-5863_1761-5860delinsATTG XP_005263235.1:n.1761-5863_1761-5860delin...
XM_006714288.4:c.1761-5863_1761-5860delinsATTG XP_006714351.1:n.1761-5863_1761-5860delin...
NM_022475.3:c.1761-5863_1761-5860delinsATTG MANE Select NP_071920.1:n.1761-5863_1761-5860delinsAT...