Canonical Allele Identifier: CA1542244453

Gene: GHR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.42629069G= , CM000667.2:g.42629069G=	GRCh38
NC_000005.9:g.42629171G= , CM000667.1:g.42629171G=	GRCh37
NC_000005.8:g.42664928G=	NCBI36
NG_011688.1:g.210146G=
NG_011688.2:g.210146G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000163.5:c.102G= MANE Select	NP_000154.1:p.Trp34=
ENST00000230882.9:c.102G= MANE Select	ENSP00000230882.4:p.Trp34=
NM_000163.4:c.102G=	NP_000154.1:p.Trp34=
NM_001242399.2:c.123G=	NP_001229328.1:p.Trp41=
NM_001242400.2:c.102G=	NP_001229329.1:p.Trp34=
NM_001242401.3:c.102G=	NP_001229330.1:p.Trp34=
NM_001242401.4:c.102G=	NP_001229330.1:p.Trp34=
NM_001242402.2:c.102G=	NP_001229331.1:p.Trp34=
NM_001242403.2:c.102G=	NP_001229332.1:p.Trp34=
NM_001242403.3:c.102G=	NP_001229332.1:p.Trp34=
NM_001242404.2:c.102G=	NP_001229333.1:p.Trp34=
NM_001242405.2:c.102G=	NP_001229334.1:p.Trp34=
NM_001242406.2:c.102G=	NP_001229335.1:p.Trp34=
NM_001242460.1:c.71-59821G=	NP_001229389.1:n.71-59821G=
NM_001242462.1:c.102G=	NP_001229391.1:p.Trp34=
ENST00000230882.8:c.102G=	ENSP00000230882.4:p.Trp34=
ENST00000357703.6:c.71-59821G=	ENSP00000350335.3:n.71-59821G=
ENST00000511135.5:c.102G=	ENSP00000422333.1:p.Trp34=
ENST00000513671.5:c.102G=	ENSP00000426739.1:p.Trp34=
ENST00000537449.5:c.102G=	ENSP00000442206.2:p.Trp34=
ENST00000612382.4:c.102G=	ENSP00000478332.1:p.Trp34=
ENST00000612626.4:c.102G=	ENSP00000479846.1:p.Trp34=
ENST00000615111.4:c.102G=	ENSP00000478291.1:p.Trp34=
ENST00000618088.4:c.102G=	ENSP00000482373.1:p.Trp34=
ENST00000620156.4:c.123G=	ENSP00000483403.1:p.Trp41=
ENST00000622294.2:c.102G=	ENSP00000483926.1:p.Trp34=
XM_011514031.1:c.92-59821G=	XP_011512333.1:n.92-59821G=