Canonical Allele Identifier: CA1420511875
Gene: GHSR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448304_172448307delinsAGCT , CM000665.2:g.172448304_172448307delinsAGCT GRCh38
NC_000003.11:g.172166094_172166097delinsAGCT , CM000665.1:g.172166094_172166097delinsAGCT GRCh37
NC_000003.10:g.173648788_173648791delinsAGCT NCBI36
NG_021159.1:g.5150_5153delinsAGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.107_110delinsAGCT MANE Select ENSP00000241256.2:p.Gln36=
ENST00000241256.2:c.107_110delinsAGCT ENSP00000241256.2:p.Gln36=
ENST00000427970.1:c.107_110delinsAGCT ENSP00000395344.1:p.Gln36=
NM_004122.2:c.107_110delinsAGCT NP_004113.1:p.Gln36=
NM_198407.2:c.107_110delinsAGCT MANE Select NP_940799.1:p.Gln36=
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