Canonical Allele Identifier: CA2683363265
Gene: HIP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.75582008del , CM000669.2:g.75582008del GRCh38
NC_000007.13:g.75211324del , CM000669.1:g.75211324del GRCh37
NC_000007.12:g.75049260del NCBI36
NG_023251.2:g.161956del
NG_023251.3:g.161956del

Transcript Alleles

HGVS Amino-acid Change
ENST00000336926.11:c.542+69del MANE Select ENSP00000336747.6:n.542+69del
ENST00000336926.10:c.542+69del ENSP00000336747.6:n.542+69del
ENST00000434438.6:c.542+69del ENSP00000410300.2:n.542+69del
ENST00000616821.4:c.455+69del ENSP00000484528.1:n.455+69del
NM_001243198.2:c.542+69del NP_001230127.1:n.542+69del
NM_005338.6:c.542+69del NP_005329.3:n.542+69del
XM_005250304.2:c.455+69del XP_005250361.1:n.455+69del
XM_005250305.2:c.440+69del XP_005250362.1:n.440+69del
XM_011516116.1:c.542+69del XP_011514418.1:n.542+69del
XM_011516116.2:c.542+69del XP_011514418.1:n.542+69del
XM_017012099.1:c.500+69del XP_016867588.1:n.500+69del
NM_005338.7:c.542+69del MANE Select NP_005329.3:n.542+69del
NM_001243198.3:c.542+69del NP_001230127.1:n.542+69del
NM_001382444.1:c.440+69del NP_001369373.1:n.440+69del
NM_001382445.1:c.455+69del NP_001369374.1:n.455+69del