Canonical Allele Identifier: CA2580069087
Gene: GHSR HGNC NCBI

Linked Data

ClinVar Variation Id: 2011495
ClinVar RCV Id: RCV002829550

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448359_172448360delinsCT , CM000665.2:g.172448359_172448360delinsCT GRCh38
NC_000003.11:g.172166149_172166150delinsCT , CM000665.1:g.172166149_172166150delinsCT GRCh37
NC_000003.10:g.173648843_173648844delinsCT NCBI36
NG_021159.1:g.5097_5098delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000241256.3:c.54_55delinsAG MANE Select ENSP00000241256.2:p.Asp18_Leu19delinsGluV...
ENST00000241256.2:c.54_55delinsAG ENSP00000241256.2:p.Asp18_Leu19delinsGluV...
ENST00000427970.1:c.54_55delinsAG ENSP00000395344.1:p.Asp18_Leu19delinsGluV...
NM_004122.2:c.54_55delinsAG NP_004113.1:p.Asp18_Leu19delinsGluVal
NM_198407.2:c.54_55delinsAG MANE Select NP_940799.1:p.Asp18_Leu19delinsGluVal