Canonical Allele Identifier: CA2707459027

Gene: HHIP

Linked Data

• dbSNP Id: rs2126683181

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.144728747C>T , CM000666.2:g.144728747C>T	GRCh38
NC_000004.11:g.145649899C>T , CM000666.1:g.145649899C>T	GRCh37
NC_000004.10:g.145869349C>T	NCBI36
NG_011496.1:g.87727C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296575.8:c.1761-5994C>T MANE Select	ENSP00000296575.3:n.1761-5994C>T
ENST00000649263.1:c.328-312769G>A	ENSP00000497507.1:n.328-312769G>A
ENST00000296575.7:c.1761-5994C>T	ENSP00000296575.3:n.1761-5994C>T
NM_022475.2:c.1761-5994C>T	NP_071920.1:n.1761-5994C>T
XM_005263178.3:c.1761-5994C>T	XP_005263235.1:n.1761-5994C>T
XM_006714288.2:c.1761-5994C>T	XP_006714351.1:n.1761-5994C>T
XM_005263178.5:c.1761-5994C>T	XP_005263235.1:n.1761-5994C>T
XM_006714288.4:c.1761-5994C>T	XP_006714351.1:n.1761-5994C>T
NM_022475.3:c.1761-5994C>T MANE Select	NP_071920.1:n.1761-5994C>T