Canonical Allele Identifier: CA1717985638

Gene: HIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75582137_75582138delinsTG , CM000669.2:g.75582137_75582138delinsTG	GRCh38
NC_000007.13:g.75211453_75211454delinsTG , CM000669.1:g.75211453_75211454delinsTG	GRCh37
NC_000007.12:g.75049389_75049390delinsTG	NCBI36
NG_023251.2:g.161824_161825delinsCA
NG_023251.3:g.161824_161825delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336926.11:c.479_480delinsCA MANE Select	ENSP00000336747.6:p.Pro160=
ENST00000336926.10:c.479_480delinsCA	ENSP00000336747.6:p.Pro160=
ENST00000420909.1:c.392_393delinsCA	ENSP00000414280.1:p.Pro131=
ENST00000434438.6:c.479_480delinsCA	ENSP00000410300.2:p.Pro160=
ENST00000616821.4:c.392_393delinsCA	ENSP00000484528.1:p.Pro131=
NM_001243198.2:c.479_480delinsCA	NP_001230127.1:p.Pro160=
NM_005338.6:c.479_480delinsCA	NP_005329.3:p.Pro160=
XM_005250304.2:c.392_393delinsCA	XP_005250361.1:p.Pro131=
XM_005250305.2:c.377_378delinsCA	XP_005250362.1:p.Pro126=
XM_011516116.1:c.479_480delinsCA	XP_011514418.1:p.Pro160=
XM_011516116.2:c.479_480delinsCA	XP_011514418.1:p.Pro160=
XM_017012099.1:c.437_438delinsCA	XP_016867588.1:p.Pro146=
NM_005338.7:c.479_480delinsCA MANE Select	NP_005329.3:p.Pro160=
NM_001243198.3:c.479_480delinsCA	NP_001230127.1:p.Pro160=
NM_001382444.1:c.377_378delinsCA	NP_001369373.1:p.Pro126=
NM_001382445.1:c.392_393delinsCA	NP_001369374.1:p.Pro131=