Canonical Allele Identifier: CA1500800297

Gene: HHIP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.144728710A= , CM000666.2:g.144728710A=	GRCh38
NC_000004.11:g.145649862A= , CM000666.1:g.145649862A=	GRCh37
NC_000004.10:g.145869312A=	NCBI36
NG_011496.1:g.87690A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296575.8:c.1761-6031A= MANE Select	ENSP00000296575.3:n.1761-6031A=
ENST00000649263.1:c.328-312732T=	ENSP00000497507.1:n.328-312732T=
ENST00000296575.7:c.1761-6031A=	ENSP00000296575.3:n.1761-6031A=
NM_022475.2:c.1761-6031A=	NP_071920.1:n.1761-6031A=
XM_005263178.3:c.1761-6031A=	XP_005263235.1:n.1761-6031A=
XM_006714288.2:c.1761-6031A=	XP_006714351.1:n.1761-6031A=
XM_005263178.5:c.1761-6031A=	XP_005263235.1:n.1761-6031A=
XM_006714288.4:c.1761-6031A=	XP_006714351.1:n.1761-6031A=
NM_022475.3:c.1761-6031A= MANE Select	NP_071920.1:n.1761-6031A=