Canonical Allele Identifier: CA10624877

Gene: GHR

Linked Data

• ClinVar Variation Id: 353688
• ClinVar RCV Id: RCV000301981
• dbSNP Id: rs886060643
• MyVariant Identifiers: chr5:g.42719397C>G (hg19) ; chr5:g.42719295C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.42719295C>G , CM000667.2:g.42719295C>G	GRCh38
NC_000005.9:g.42719397C>G , CM000667.1:g.42719397C>G	GRCh37
NC_000005.8:g.42755154C>G	NCBI36
NG_011688.1:g.300372C>G
NG_011688.2:g.300372C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230882.9:c.1788C>G MANE Select	ENSP00000230882.4:p.Thr596=
ENST00000230882.8:c.1788C>G	ENSP00000230882.4:p.Thr596=
ENST00000357703.6:c.1722C>G	ENSP00000350335.3:p.Thr574=
ENST00000511135.5:c.*1400C>G	ENSP00000422333.1:n.*1400C>G
ENST00000537449.5:c.1788C>G	ENSP00000442206.2:p.Thr596=
ENST00000612382.4:c.1788C>G	ENSP00000478332.1:p.Thr596=
ENST00000612626.4:c.1788C>G	ENSP00000479846.1:p.Thr596=
ENST00000615111.4:c.1788C>G	ENSP00000478291.1:p.Thr596=
ENST00000618088.4:c.1788C>G	ENSP00000482373.1:p.Thr596=
ENST00000620156.4:c.1809C>G	ENSP00000483403.1:p.Thr603=
ENST00000622294.2:c.*830C>G	ENSP00000483926.1:n.*830C>G
NM_000163.4:c.1788C>G	NP_000154.1:p.Thr596=
NM_001242399.2:c.1809C>G	NP_001229328.1:p.Thr603=
NM_001242400.2:c.1788C>G	NP_001229329.1:p.Thr596=
NM_001242401.3:c.1788C>G	NP_001229330.1:p.Thr596=
NM_001242402.2:c.1788C>G	NP_001229331.1:p.Thr596=
NM_001242403.2:c.1788C>G	NP_001229332.1:p.Thr596=
NM_001242404.2:c.1788C>G	NP_001229333.1:p.Thr596=
NM_001242405.2:c.1788C>G	NP_001229334.1:p.Thr596=
NM_001242406.2:c.1788C>G	NP_001229335.1:p.Thr596=
NM_001242460.1:c.1722C>G	NP_001229389.1:p.Thr574=
NM_001242462.1:c.*830C>G	NP_001229391.1:n.*830C>G
XM_011514031.1:c.1743C>G	XP_011512333.1:p.Thr581=
NM_000163.5:c.1788C>G MANE Select	NP_000154.1:p.Thr596=
NM_001242401.4:c.1788C>G	NP_001229330.1:p.Thr596=
NM_001242403.3:c.1788C>G	NP_001229332.1:p.Thr596=