Canonical Allele Identifier: CA1500751370

Gene: HHIP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.144647200T= , CM000666.2:g.144647200T=	GRCh38
NC_000004.11:g.145568352T= , CM000666.1:g.145568352T=	GRCh37
NC_000004.10:g.145787802T=	NCBI36
NG_011496.1:g.6180T=

Transcript Alleles

HGVS	Amino-acid Change
NM_022475.3:c.279+246T= MANE Select	NP_071920.1:n.279+246T=
ENST00000296575.8:c.279+246T= MANE Select	ENSP00000296575.3:n.279+246T=
NM_022475.2:c.279+246T=	NP_071920.1:n.279+246T=
ENST00000296575.7:c.279+246T=	ENSP00000296575.3:n.279+246T=
ENST00000434550.2:c.279+246T=	ENSP00000408587.2:n.279+246T=
ENST00000505891.5:n.102T=
ENST00000649263.1:c.328-231222A=	ENSP00000497507.1:n.328-231222A=
XM_005263178.3:c.279+246T=	XP_005263235.1:n.279+246T=
XM_005263178.5:c.279+246T=	XP_005263235.1:n.279+246T=
XM_006714288.2:c.279+246T=	XP_006714351.1:n.279+246T=
XM_006714288.4:c.279+246T=	XP_006714351.1:n.279+246T=