Canonical Allele Identifier: CA2668560151
Gene: GHSR HGNC NCBI

Linked Data

gnomAD v4: 3-172448142-AGCAGATCGGAGAAGGCCATGCTGGACAGGTAGAGGTTGGTGGTGGTGC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448147_172448194del , CM000665.2:g.172448147_172448194del GRCh38
NC_000003.11:g.172165937_172165984del , CM000665.1:g.172165937_172165984del GRCh37
NC_000003.10:g.173648631_173648678del NCBI36
NG_021159.1:g.5267_5314del

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.224_271del MANE Select ENSP00000241256.2:p.Arg75_Leu90del
ENST00000241256.2:c.224_271del ENSP00000241256.2:p.Arg75_Leu90del
ENST00000427970.1:c.224_271del ENSP00000395344.1:p.Arg75_Leu90del
NM_004122.2:c.224_271del NP_004113.1:p.Arg75_Leu90del
NM_198407.2:c.224_271del MANE Select NP_940799.1:p.Arg75_Leu90del
Search 100 bp 5'
Search 100 bp 3'