Canonical Allele Identifier: CA1420511871
Gene: GHSR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448296_172448297delinsCG , CM000665.2:g.172448296_172448297delinsCG GRCh38
NC_000003.11:g.172166086_172166087delinsCG , CM000665.1:g.172166086_172166087delinsCG GRCh37
NC_000003.10:g.173648780_173648781delinsCG NCBI36
NG_021159.1:g.5160_5161delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.117_118delinsCG MANE Select ENSP00000241256.2:p.Pro39=
ENST00000241256.2:c.117_118delinsCG ENSP00000241256.2:p.Pro39=
ENST00000427970.1:c.117_118delinsCG ENSP00000395344.1:p.Pro39=
NM_004122.2:c.117_118delinsCG NP_004113.1:p.Pro39=
NM_198407.2:c.117_118delinsCG MANE Select NP_940799.1:p.Pro39=
Search 100 bp 5'
Search 100 bp 3'