Canonical Allele Identifier: CA1500800297
Gene: HHIP HGNC NCBI

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=