Canonical Allele Identifier: CA1420511784
Gene: GHSR HGNC NCBI

Linked Data

dbSNP Id: rs1737526396

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448130del , CM000665.2:g.172448130del GRCh38
NC_000003.11:g.172165920del , CM000665.1:g.172165920del GRCh37
NC_000003.10:g.173648614del NCBI36
NG_021159.1:g.5327del

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.284del MANE Select ENSP00000241256.2:p.Cys95SerfsTer?
ENST00000241256.2:c.284del ENSP00000241256.2:p.Cys95SerfsTer?
ENST00000427970.1:c.284del ENSP00000395344.1:p.Cys95SerfsTer?
NM_004122.2:c.284del NP_004113.1:p.Cys95SerfsTer?
NM_198407.2:c.284del MANE Select NP_940799.1:p.Cys95SerfsTer?