Canonical Allele Identifier: CA2580610841
Gene: GHSR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448116_172448117delinsAT , CM000665.2:g.172448116_172448117delinsAT GRCh38
NC_000003.11:g.172165906_172165907delinsAT , CM000665.1:g.172165906_172165907delinsAT GRCh37
NC_000003.10:g.173648600_173648601delinsAT NCBI36
NG_021159.1:g.5340_5341delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.297_298delinsAT MANE Select ENSP00000241256.2:p.Asp99_Leu100delinsGluPhe
ENST00000241256.2:c.297_298delinsAT ENSP00000241256.2:p.Asp99_Leu100delinsGluPhe
ENST00000427970.1:c.297_298delinsAT ENSP00000395344.1:p.Asp99_Leu100delinsGluPhe
NM_004122.2:c.297_298delinsAT NP_004113.1:p.Asp99_Leu100delinsGluPhe
NM_198407.2:c.297_298delinsAT MANE Select NP_940799.1:p.Asp99_Leu100delinsGluPhe
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