Canonical Allele Identifier: CA107721190

Gene: HHIP

Linked Data

• dbSNP Id: rs747583855
• MyVariant Identifiers: chr4:g.145650096A>G (hg19) ; chr4:g.144728944A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.144728944A>G , CM000666.2:g.144728944A>G	GRCh38
NC_000004.11:g.145650096A>G , CM000666.1:g.145650096A>G	GRCh37
NC_000004.10:g.145869546A>G	NCBI36
NG_011496.1:g.87924A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000296575.8:c.1761-5797A>G MANE Select	ENSP00000296575.3:n.1761-5797A>G
ENST00000649263.1:c.328-312966T>C	ENSP00000497507.1:n.328-312966T>C
ENST00000296575.7:c.1761-5797A>G	ENSP00000296575.3:n.1761-5797A>G
NM_022475.2:c.1761-5797A>G	NP_071920.1:n.1761-5797A>G
XM_005263178.3:c.1761-5797A>G	XP_005263235.1:n.1761-5797A>G
XM_006714288.2:c.1761-5797A>G	XP_006714351.1:n.1761-5797A>G
XM_005263178.5:c.1761-5797A>G	XP_005263235.1:n.1761-5797A>G
XM_006714288.4:c.1761-5797A>G	XP_006714351.1:n.1761-5797A>G
NM_022475.3:c.1761-5797A>G MANE Select	NP_071920.1:n.1761-5797A>G