Canonical Allele Identifier: CA1500800461

Gene: HHIP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.144728900_144728901delinsAC , CM000666.2:g.144728900_144728901delinsAC	GRCh38
NC_000004.11:g.145650052_145650053delinsAC , CM000666.1:g.145650052_145650053delinsAC	GRCh37
NC_000004.10:g.145869502_145869503delinsAC	NCBI36
NG_011496.1:g.87880_87881delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296575.8:c.1761-5841_1761-5840delinsAC MANE Select	ENSP00000296575.3:n.1761-5841_1761-5840delinsAC
ENST00000649263.1:c.328-312923_328-312922delinsGT	ENSP00000497507.1:n.328-312923_328-312922delinsGT
ENST00000296575.7:c.1761-5841_1761-5840delinsAC	ENSP00000296575.3:n.1761-5841_1761-5840delinsAC
NM_022475.2:c.1761-5841_1761-5840delinsAC	NP_071920.1:n.1761-5841_1761-5840delinsAC
XM_005263178.3:c.1761-5841_1761-5840delinsAC	XP_005263235.1:n.1761-5841_1761-5840delinsAC
XM_006714288.2:c.1761-5841_1761-5840delinsAC	XP_006714351.1:n.1761-5841_1761-5840delinsAC
XM_005263178.5:c.1761-5841_1761-5840delinsAC	XP_005263235.1:n.1761-5841_1761-5840delinsAC
XM_006714288.4:c.1761-5841_1761-5840delinsAC	XP_006714351.1:n.1761-5841_1761-5840delinsAC
NM_022475.3:c.1761-5841_1761-5840delinsAC MANE Select	NP_071920.1:n.1761-5841_1761-5840delinsAC