Canonical Allele Identifier: CA107721107
Gene: HHIP HGNC NCBI

Linked Data

dbSNP Id: rs1017586649

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144728856C>T , CM000666.2:g.144728856C>T GRCh38
NC_000004.11:g.145650008C>T , CM000666.1:g.145650008C>T GRCh37
NC_000004.10:g.145869458C>T NCBI36
NG_011496.1:g.87836C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296575.8:c.1761-5885C>T MANE Select ENSP00000296575.3:n.1761-5885C>T
ENST00000649263.1:c.328-312878G>A ENSP00000497507.1:n.328-312878G>A
ENST00000296575.7:c.1761-5885C>T ENSP00000296575.3:n.1761-5885C>T
NM_022475.2:c.1761-5885C>T NP_071920.1:n.1761-5885C>T
XM_005263178.3:c.1761-5885C>T XP_005263235.1:n.1761-5885C>T
XM_006714288.2:c.1761-5885C>T XP_006714351.1:n.1761-5885C>T
XM_005263178.5:c.1761-5885C>T XP_005263235.1:n.1761-5885C>T
XM_006714288.4:c.1761-5885C>T XP_006714351.1:n.1761-5885C>T
NM_022475.3:c.1761-5885C>T MANE Select NP_071920.1:n.1761-5885C>T