Canonical Allele Identifier: CA367727180
Gene: HIP1 HGNC NCBI

Linked Data

dbSNP Id: rs587675702

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.75582114C>G , CM000669.2:g.75582114C>G GRCh38
NC_000007.13:g.75211430C>G , CM000669.1:g.75211430C>G GRCh37
NC_000007.12:g.75049366C>G NCBI36
NG_023251.2:g.161848G>C
NG_023251.3:g.161848G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000336926.11:c.503G>C MANE Select ENSP00000336747.6:p.Arg168Pro
ENST00000336926.10:c.503G>C ENSP00000336747.6:p.Arg168Pro
ENST00000420909.1:c.416G>C ENSP00000414280.1:p.Arg139Pro
ENST00000434438.6:c.503G>C ENSP00000410300.2:p.Arg168Pro
ENST00000616821.4:c.416G>C ENSP00000484528.1:p.Arg139Pro
NM_001243198.2:c.503G>C NP_001230127.1:p.Arg168Pro
NM_005338.6:c.503G>C NP_005329.3:p.Arg168Pro
XM_005250304.2:c.416G>C XP_005250361.1:p.Arg139Pro
XM_005250305.2:c.401G>C XP_005250362.1:p.Arg134Pro
XM_011516116.1:c.503G>C XP_011514418.1:p.Arg168Pro
XM_011516116.2:c.503G>C XP_011514418.1:p.Arg168Pro
XM_017012099.1:c.461G>C XP_016867588.1:p.Arg154Pro
NM_005338.7:c.503G>C MANE Select NP_005329.3:p.Arg168Pro
NM_001243198.3:c.503G>C NP_001230127.1:p.Arg168Pro
NM_001382444.1:c.401G>C NP_001369373.1:p.Arg134Pro
NM_001382445.1:c.416G>C NP_001369374.1:p.Arg139Pro