Canonical Allele Identifier: CA1069058404

Gene: HHIP

Linked Data

• dbSNP Id: rs1730866276
• gnomAD v3: 4-144728708-G-GA
• gnomAD v4: 4-144728708-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.144728713dup , CM000666.2:g.144728713dup	GRCh38
NC_000004.11:g.145649865dup , CM000666.1:g.145649865dup	GRCh37
NC_000004.10:g.145869315dup	NCBI36
NG_011496.1:g.87693dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296575.8:c.1761-6028dup MANE Select	ENSP00000296575.3:n.1761-6028dup
ENST00000649263.1:c.328-312731dup	ENSP00000497507.1:n.328-312731dup
ENST00000296575.7:c.1761-6028dup	ENSP00000296575.3:n.1761-6028dup
NM_022475.2:c.1761-6028dup	NP_071920.1:n.1761-6028dup
XM_005263178.3:c.1761-6028dup	XP_005263235.1:n.1761-6028dup
XM_006714288.2:c.1761-6028dup	XP_006714351.1:n.1761-6028dup
XM_005263178.5:c.1761-6028dup	XP_005263235.1:n.1761-6028dup
XM_006714288.4:c.1761-6028dup	XP_006714351.1:n.1761-6028dup
NM_022475.3:c.1761-6028dup MANE Select	NP_071920.1:n.1761-6028dup