Canonical Allele Identifier: CA1500800438
Gene: HHIP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144728878A= , CM000666.2:g.144728878A= GRCh38
NC_000004.11:g.145650030A= , CM000666.1:g.145650030A= GRCh37
NC_000004.10:g.145869480A= NCBI36
NG_011496.1:g.87858A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296575.8:c.1761-5863A= MANE Select ENSP00000296575.3:n.1761-5863A=
ENST00000649263.1:c.328-312900T= ENSP00000497507.1:n.328-312900T=
ENST00000296575.7:c.1761-5863A= ENSP00000296575.3:n.1761-5863A=
NM_022475.2:c.1761-5863A= NP_071920.1:n.1761-5863A=
XM_005263178.3:c.1761-5863A= XP_005263235.1:n.1761-5863A=
XM_006714288.2:c.1761-5863A= XP_006714351.1:n.1761-5863A=
XM_005263178.5:c.1761-5863A= XP_005263235.1:n.1761-5863A=
XM_006714288.4:c.1761-5863A= XP_006714351.1:n.1761-5863A=
NM_022475.3:c.1761-5863A= MANE Select NP_071920.1:n.1761-5863A=
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