Canonical Allele Identifier: CA1542195888

Gene: GHR

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.42489040A>G , CM000667.2:g.42489040A>G	GRCh38
NC_000005.9:g.42489142A>G , CM000667.1:g.42489142A>G	GRCh37
NC_000005.8:g.42524899A>G	NCBI36
NG_011688.1:g.70117A>G
NG_011688.2:g.70117A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230882.9:c.-12+65085A>G MANE Select	ENSP00000230882.4:n.-12+65085A>G
ENST00000230882.8:c.-12+65085A>G	ENSP00000230882.4:n.-12+65085A>G
ENST00000513671.5:c.-12+64442A>G	ENSP00000426739.1:n.-12+64442A>G
ENST00000615111.4:c.-296-25040A>G	ENSP00000478291.1:n.-296-25040A>G
ENST00000620156.4:c.10+64442A>G	ENSP00000483403.1:n.10+64442A>G
NM_000163.4:c.-12+65085A>G	NP_000154.1:n.-12+65085A>G
NM_001242399.2:c.10+64442A>G	NP_001229328.1:n.10+64442A>G
NM_001242400.2:c.-296-25040A>G	NP_001229329.1:n.-296-25040A>G
NM_001242401.3:c.-12+5711A>G	NP_001229330.1:n.-12+5711A>G
XM_011514031.1:c.10+64442A>G	XP_011512333.1:n.10+64442A>G
NM_000163.5:c.-12+65085A>G MANE Select	NP_000154.1:n.-12+65085A>G
NM_001242401.4:c.-12+5711A>G	NP_001229330.1:n.-12+5711A>G