Canonical Allele Identifier: CA1542287665
Gene: GHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.42694903_42694904delinsAC , CM000667.2:g.42694903_42694904delinsAC GRCh38
NC_000005.9:g.42695005_42695006delinsAC , CM000667.1:g.42695005_42695006delinsAC GRCh37
NC_000005.8:g.42730762_42730763delinsAC NCBI36
NG_011688.1:g.275980_275981delinsAC
NG_011688.2:g.275980_275981delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000230882.9:c.267-14_267-13delinsAC MANE Select ENSP00000230882.4:n.267-14_267-13delinsAC
ENST00000230882.8:c.267-14_267-13delinsAC ENSP00000230882.4:n.267-14_267-13delinsAC
ENST00000357703.6:c.201-14_201-13delinsAC ENSP00000350335.3:n.201-14_201-13delinsAC
ENST00000511135.5:c.137-14_137-13delinsAC ENSP00000422333.1:n.137-14_137-13delinsAC
ENST00000537449.5:c.267-14_267-13delinsAC ENSP00000442206.2:n.267-14_267-13delinsAC
ENST00000612382.4:c.267-14_267-13delinsAC ENSP00000478332.1:n.267-14_267-13delinsAC
ENST00000612626.4:c.267-14_267-13delinsAC ENSP00000479846.1:n.267-14_267-13delinsAC
ENST00000615111.4:c.267-14_267-13delinsAC ENSP00000478291.1:n.267-14_267-13delinsAC
ENST00000618088.4:c.267-14_267-13delinsAC ENSP00000482373.1:n.267-14_267-13delinsAC
ENST00000620156.4:c.288-14_288-13delinsAC ENSP00000483403.1:n.288-14_288-13delinsAC
ENST00000622294.2:c.267-14_267-13delinsAC ENSP00000483926.1:n.267-14_267-13delinsAC
NM_000163.4:c.267-14_267-13delinsAC NP_000154.1:n.267-14_267-13delinsAC
NM_001242399.2:c.288-14_288-13delinsAC NP_001229328.1:n.288-14_288-13delinsAC
NM_001242400.2:c.267-14_267-13delinsAC NP_001229329.1:n.267-14_267-13delinsAC
NM_001242401.3:c.267-14_267-13delinsAC NP_001229330.1:n.267-14_267-13delinsAC
NM_001242402.2:c.267-14_267-13delinsAC NP_001229331.1:n.267-14_267-13delinsAC
NM_001242403.2:c.267-14_267-13delinsAC NP_001229332.1:n.267-14_267-13delinsAC
NM_001242404.2:c.267-14_267-13delinsAC NP_001229333.1:n.267-14_267-13delinsAC
NM_001242405.2:c.267-14_267-13delinsAC NP_001229334.1:n.267-14_267-13delinsAC
NM_001242406.2:c.267-14_267-13delinsAC NP_001229335.1:n.267-14_267-13delinsAC
NM_001242460.1:c.201-14_201-13delinsAC NP_001229389.1:n.201-14_201-13delinsAC
NM_001242462.1:c.267-14_267-13delinsAC NP_001229391.1:n.267-14_267-13delinsAC
XM_011514031.1:c.222-14_222-13delinsAC XP_011512333.1:n.222-14_222-13delinsAC
NM_000163.5:c.267-14_267-13delinsAC MANE Select NP_000154.1:n.267-14_267-13delinsAC
NM_001242401.4:c.267-14_267-13delinsAC NP_001229330.1:n.267-14_267-13delinsAC
NM_001242403.3:c.267-14_267-13delinsAC NP_001229332.1:n.267-14_267-13delinsAC