Canonical Allele Identifier: CA359695513

Gene: GHR

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.42699888T>A , CM000667.2:g.42699888T>A	GRCh38
NC_000005.9:g.42699990T>A , CM000667.1:g.42699990T>A	GRCh37
NC_000005.8:g.42735747T>A	NCBI36
NG_011688.1:g.280965T>A
NG_011688.2:g.280965T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230882.9:c.504T>A MANE Select	ENSP00000230882.4:p.His168Gln
ENST00000230882.8:c.504T>A	ENSP00000230882.4:p.His168Gln
ENST00000357703.6:c.438T>A	ENSP00000350335.3:p.His146Gln
ENST00000511135.5:c.*116T>A	ENSP00000422333.1:n.*116T>A
ENST00000537449.5:c.504T>A	ENSP00000442206.2:p.His168Gln
ENST00000612382.4:c.504T>A	ENSP00000478332.1:p.His168Gln
ENST00000612626.4:c.504T>A	ENSP00000479846.1:p.His168Gln
ENST00000615111.4:c.504T>A	ENSP00000478291.1:p.His168Gln
ENST00000618088.4:c.504T>A	ENSP00000482373.1:p.His168Gln
ENST00000620156.4:c.525T>A	ENSP00000483403.1:p.His175Gln
ENST00000622294.2:c.504T>A	ENSP00000483926.1:p.His168Gln
NM_000163.4:c.504T>A	NP_000154.1:p.His168Gln
NM_001242399.2:c.525T>A	NP_001229328.1:p.His175Gln
NM_001242400.2:c.504T>A	NP_001229329.1:p.His168Gln
NM_001242401.3:c.504T>A	NP_001229330.1:p.His168Gln
NM_001242402.2:c.504T>A	NP_001229331.1:p.His168Gln
NM_001242403.2:c.504T>A	NP_001229332.1:p.His168Gln
NM_001242404.2:c.504T>A	NP_001229333.1:p.His168Gln
NM_001242405.2:c.504T>A	NP_001229334.1:p.His168Gln
NM_001242406.2:c.504T>A	NP_001229335.1:p.His168Gln
NM_001242460.1:c.438T>A	NP_001229389.1:p.His146Gln
NM_001242462.1:c.504T>A	NP_001229391.1:p.His168Gln
XM_011514031.1:c.459T>A	XP_011512333.1:p.His153Gln
NM_000163.5:c.504T>A MANE Select	NP_000154.1:p.His168Gln
NM_001242401.4:c.504T>A	NP_001229330.1:p.His168Gln
NM_001242403.3:c.504T>A	NP_001229332.1:p.His168Gln