Canonical Allele Identifier: CA2581400141

Gene: HHIP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.144728869G>C , CM000666.2:g.144728869G>C	GRCh38
NC_000004.11:g.145650021G>C , CM000666.1:g.145650021G>C	GRCh37
NC_000004.10:g.145869471G>C	NCBI36
NG_011496.1:g.87849G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000296575.8:c.1761-5872G>C MANE Select	ENSP00000296575.3:n.1761-5872G>C
ENST00000649263.1:c.328-312891C>G	ENSP00000497507.1:n.328-312891C>G
ENST00000296575.7:c.1761-5872G>C	ENSP00000296575.3:n.1761-5872G>C
NM_022475.2:c.1761-5872G>C	NP_071920.1:n.1761-5872G>C
XM_005263178.3:c.1761-5872G>C	XP_005263235.1:n.1761-5872G>C
XM_006714288.2:c.1761-5872G>C	XP_006714351.1:n.1761-5872G>C
XM_005263178.5:c.1761-5872G>C	XP_005263235.1:n.1761-5872G>C
XM_006714288.4:c.1761-5872G>C	XP_006714351.1:n.1761-5872G>C
NM_022475.3:c.1761-5872G>C MANE Select	NP_071920.1:n.1761-5872G>C