Canonical Allele Identifier: CA1500800552

Gene: HHIP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.144728989_144728990delinsAG , CM000666.2:g.144728989_144728990delinsAG	GRCh38
NC_000004.11:g.145650141_145650142delinsAG , CM000666.1:g.145650141_145650142delinsAG	GRCh37
NC_000004.10:g.145869591_145869592delinsAG	NCBI36
NG_011496.1:g.87969_87970delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296575.8:c.1761-5752_1761-5751delinsAG MANE Select	ENSP00000296575.3:n.1761-5752_1761-5751delinsAG
ENST00000649263.1:c.328-313012_328-313011delinsCT	ENSP00000497507.1:n.328-313012_328-313011delinsCT
ENST00000296575.7:c.1761-5752_1761-5751delinsAG	ENSP00000296575.3:n.1761-5752_1761-5751delinsAG
NM_022475.2:c.1761-5752_1761-5751delinsAG	NP_071920.1:n.1761-5752_1761-5751delinsAG
XM_005263178.3:c.1761-5752_1761-5751delinsAG	XP_005263235.1:n.1761-5752_1761-5751delinsAG
XM_006714288.2:c.1761-5752_1761-5751delinsAG	XP_006714351.1:n.1761-5752_1761-5751delinsAG
XM_005263178.5:c.1761-5752_1761-5751delinsAG	XP_005263235.1:n.1761-5752_1761-5751delinsAG
XM_006714288.4:c.1761-5752_1761-5751delinsAG	XP_006714351.1:n.1761-5752_1761-5751delinsAG
NM_022475.3:c.1761-5752_1761-5751delinsAG MANE Select	NP_071920.1:n.1761-5752_1761-5751delinsAG