Canonical Allele Identifier: CA1069058411

Gene: HHIP

Linked Data

• gnomAD v3: 4-144728740-A-AGTGTAG
• gnomAD v4: 4-144728740-A-AGTGTAG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.144728740_144728741insGTGTAG , CM000666.2:g.144728740_144728741insGTGTAG	GRCh38
NC_000004.11:g.145649892_145649893insGTGTAG , CM000666.1:g.145649892_145649893insGTGTAG	GRCh37
NC_000004.10:g.145869342_145869343insGTGTAG	NCBI36
NG_011496.1:g.87720_87721insGTGTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296575.8:c.1761-6001_1761-6000insGTGTAG MANE Select	ENSP00000296575.3:n.1761-6001_1761-6000insGTGTAG
ENST00000649263.1:c.328-312763_328-312762insCTACAC	ENSP00000497507.1:n.328-312763_328-312762insCTACAC
ENST00000296575.7:c.1761-6001_1761-6000insGTGTAG	ENSP00000296575.3:n.1761-6001_1761-6000insGTGTAG
NM_022475.2:c.1761-6001_1761-6000insGTGTAG	NP_071920.1:n.1761-6001_1761-6000insGTGTAG
XM_005263178.3:c.1761-6001_1761-6000insGTGTAG	XP_005263235.1:n.1761-6001_1761-6000insGTGTAG
XM_006714288.2:c.1761-6001_1761-6000insGTGTAG	XP_006714351.1:n.1761-6001_1761-6000insGTGTAG
XM_005263178.5:c.1761-6001_1761-6000insGTGTAG	XP_005263235.1:n.1761-6001_1761-6000insGTGTAG
XM_006714288.4:c.1761-6001_1761-6000insGTGTAG	XP_006714351.1:n.1761-6001_1761-6000insGTGTAG
NM_022475.3:c.1761-6001_1761-6000insGTGTAG MANE Select	NP_071920.1:n.1761-6001_1761-6000insGTGTAG