Canonical Allele Identifier: CA2668560143
Gene: GHSR HGNC NCBI

Linked Data

gnomAD v4: 3-172447899-A-ACT
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172447899_172447900insCT , CM000665.2:g.172447899_172447900insCT GRCh38
NC_000003.11:g.172165689_172165690insCT , CM000665.1:g.172165689_172165690insCT GRCh37
NC_000003.10:g.173648383_173648384insCT NCBI36
NG_021159.1:g.5557_5558insAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.514_515insAG MANE Select ENSP00000241256.2:p.Phe172Ter
ENST00000241256.2:c.514_515insAG ENSP00000241256.2:p.Phe172Ter
ENST00000427970.1:c.514_515insAG ENSP00000395344.1:p.Phe172Ter
NM_004122.2:c.514_515insAG NP_004113.1:p.Phe172Ter
NM_198407.2:c.514_515insAG MANE Select NP_940799.1:p.Phe172Ter
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