Canonical Allele Identifier: CA788470222

Gene: HHIP

Linked Data

• dbSNP Id: rs1192116620
• MyVariant Identifiers: chr4:g.145650084_145650085insGAGTATGTTTTGTATATAAGGA (hg19) ; chr4:g.144728932_144728933insGAGTATGTTTTGTATATAAGGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.144728933_144728934insAGTATGTTTTGTATATAAGGAG , CM000666.2:g.144728933_144728934insAGTATGTTTTGTATATAAGGAG	GRCh38
NC_000004.11:g.145650085_145650086insAGTATGTTTTGTATATAAGGAG , CM000666.1:g.145650085_145650086insAGTATGTTTTGTATATAAGGAG	GRCh37
NC_000004.10:g.145869535_145869536insAGTATGTTTTGTATATAAGGAG	NCBI36
NG_011496.1:g.87913_87914insAGTATGTTTTGTATATAAGGAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000296575.8:c.1761-5808_1761-5807insAGTATGTTTTGTATATAAGGAG MANE Select	ENSP00000296575.3:n.1761-5808_1761-5807insAGTATGTTTTGTATATAAG...
ENST00000649263.1:c.328-312955_328-312954insTCCTTATATACAAAACATACTC	ENSP00000497507.1:n.328-312955_328-312954insTCCTTATATACAAAACA...
ENST00000296575.7:c.1761-5808_1761-5807insAGTATGTTTTGTATATAAGGAG	ENSP00000296575.3:n.1761-5808_1761-5807insAGTATGTTTTGTATATAAG...
NM_022475.2:c.1761-5808_1761-5807insAGTATGTTTTGTATATAAGGAG	NP_071920.1:n.1761-5808_1761-5807insAGTATGTTTTGTATATAAGGAG
XM_005263178.3:c.1761-5808_1761-5807insAGTATGTTTTGTATATAAGGAG	XP_005263235.1:n.1761-5808_1761-5807insAGTATGTTTTGTATATAAGGAG...
XM_006714288.2:c.1761-5808_1761-5807insAGTATGTTTTGTATATAAGGAG	XP_006714351.1:n.1761-5808_1761-5807insAGTATGTTTTGTATATAAGGAG...
XM_005263178.5:c.1761-5808_1761-5807insAGTATGTTTTGTATATAAGGAG	XP_005263235.1:n.1761-5808_1761-5807insAGTATGTTTTGTATATAAGGAG...
XM_006714288.4:c.1761-5808_1761-5807insAGTATGTTTTGTATATAAGGAG	XP_006714351.1:n.1761-5808_1761-5807insAGTATGTTTTGTATATAAGGAG...
NM_022475.3:c.1761-5808_1761-5807insAGTATGTTTTGTATATAAGGAG MANE Select	NP_071920.1:n.1761-5808_1761-5807insAGTATGTTTTGTATATAAGGAG