Canonical Allele Identifier: CA1542305125

Gene: GHR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.42711482_42711486delinsCAGAT , CM000667.2:g.42711482_42711486delinsCAGAT	GRCh38
NC_000005.9:g.42711584_42711588delinsCAGAT , CM000667.1:g.42711584_42711588delinsCAGAT	GRCh37
NC_000005.8:g.42747341_42747345delinsCAGAT	NCBI36
NG_011688.1:g.292559_292563delinsCAGAT
NG_011688.2:g.292559_292563delinsCAGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230882.9:c.784+110_784+114delinsCAGAT MANE Select	ENSP00000230882.4:n.784+110_784+114delinsCAGAT
ENST00000230882.8:c.784+110_784+114delinsCAGAT	ENSP00000230882.4:n.784+110_784+114delinsCAGAT
ENST00000357703.6:c.718+110_718+114delinsCAGAT	ENSP00000350335.3:n.718+110_718+114delinsCAGAT
ENST00000511135.5:c.*396+110_*396+114delinsCAGAT	ENSP00000422333.1:n.*396+110_*396+114delinsCAGAT
ENST00000537449.5:c.784+110_784+114delinsCAGAT	ENSP00000442206.2:n.784+110_784+114delinsCAGAT
ENST00000612382.4:c.784+110_784+114delinsCAGAT	ENSP00000478332.1:n.784+110_784+114delinsCAGAT
ENST00000612626.4:c.784+110_784+114delinsCAGAT	ENSP00000479846.1:n.784+110_784+114delinsCAGAT
ENST00000615111.4:c.784+110_784+114delinsCAGAT	ENSP00000478291.1:n.784+110_784+114delinsCAGAT
ENST00000618088.4:c.784+110_784+114delinsCAGAT	ENSP00000482373.1:n.784+110_784+114delinsCAGAT
ENST00000620156.4:c.805+110_805+114delinsCAGAT	ENSP00000483403.1:n.805+110_805+114delinsCAGAT
ENST00000622294.2:c.784+110_784+114delinsCAGAT	ENSP00000483926.1:n.784+110_784+114delinsCAGAT
NM_000163.4:c.784+110_784+114delinsCAGAT	NP_000154.1:n.784+110_784+114delinsCAGAT
NM_001242399.2:c.805+110_805+114delinsCAGAT	NP_001229328.1:n.805+110_805+114delinsCAGAT
NM_001242400.2:c.784+110_784+114delinsCAGAT	NP_001229329.1:n.784+110_784+114delinsCAGAT
NM_001242401.3:c.784+110_784+114delinsCAGAT	NP_001229330.1:n.784+110_784+114delinsCAGAT
NM_001242402.2:c.784+110_784+114delinsCAGAT	NP_001229331.1:n.784+110_784+114delinsCAGAT
NM_001242403.2:c.784+110_784+114delinsCAGAT	NP_001229332.1:n.784+110_784+114delinsCAGAT
NM_001242404.2:c.784+110_784+114delinsCAGAT	NP_001229333.1:n.784+110_784+114delinsCAGAT
NM_001242405.2:c.784+110_784+114delinsCAGAT	NP_001229334.1:n.784+110_784+114delinsCAGAT
NM_001242406.2:c.784+110_784+114delinsCAGAT	NP_001229335.1:n.784+110_784+114delinsCAGAT
NM_001242460.1:c.718+110_718+114delinsCAGAT	NP_001229389.1:n.718+110_718+114delinsCAGAT
NM_001242462.1:c.784+110_784+114delinsCAGAT	NP_001229391.1:n.784+110_784+114delinsCAGAT
XM_011514031.1:c.739+110_739+114delinsCAGAT	XP_011512333.1:n.739+110_739+114delinsCAGAT
NM_000163.5:c.784+110_784+114delinsCAGAT MANE Select	NP_000154.1:n.784+110_784+114delinsCAGAT
NM_001242401.4:c.784+110_784+114delinsCAGAT	NP_001229330.1:n.784+110_784+114delinsCAGAT
NM_001242403.3:c.784+110_784+114delinsCAGAT	NP_001229332.1:n.784+110_784+114delinsCAGAT