Canonical Allele Identifier: CA1500800330

Gene: HHIP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.144728761_144728763delinsTGA , CM000666.2:g.144728761_144728763delinsTGA	GRCh38
NC_000004.11:g.145649913_145649915delinsTGA , CM000666.1:g.145649913_145649915delinsTGA	GRCh37
NC_000004.10:g.145869363_145869365delinsTGA	NCBI36
NG_011496.1:g.87741_87743delinsTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296575.8:c.1761-5980_1761-5978delinsTGA MANE Select	ENSP00000296575.3:n.1761-5980_1761-5978delinsTGA
ENST00000649263.1:c.328-312785_328-312783delinsTCA	ENSP00000497507.1:n.328-312785_328-312783delinsTCA
ENST00000296575.7:c.1761-5980_1761-5978delinsTGA	ENSP00000296575.3:n.1761-5980_1761-5978delinsTGA
NM_022475.2:c.1761-5980_1761-5978delinsTGA	NP_071920.1:n.1761-5980_1761-5978delinsTGA
XM_005263178.3:c.1761-5980_1761-5978delinsTGA	XP_005263235.1:n.1761-5980_1761-5978delinsTGA
XM_006714288.2:c.1761-5980_1761-5978delinsTGA	XP_006714351.1:n.1761-5980_1761-5978delinsTGA
XM_005263178.5:c.1761-5980_1761-5978delinsTGA	XP_005263235.1:n.1761-5980_1761-5978delinsTGA
XM_006714288.4:c.1761-5980_1761-5978delinsTGA	XP_006714351.1:n.1761-5980_1761-5978delinsTGA
NM_022475.3:c.1761-5980_1761-5978delinsTGA MANE Select	NP_071920.1:n.1761-5980_1761-5978delinsTGA