Canonical Allele Identifier: CA810773000

Gene: GHR

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.42507231T>C , CM000667.2:g.42507231T>C	GRCh38
NC_000005.9:g.42507333T>C , CM000667.1:g.42507333T>C	GRCh37
NC_000005.8:g.42543090T>C	NCBI36
NG_011688.1:g.88308T>C
NG_011688.2:g.88308T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230882.9:c.-11-58633T>C MANE Select	ENSP00000230882.4:n.-11-58633T>C
ENST00000230882.8:c.-11-58633T>C	ENSP00000230882.4:n.-11-58633T>C
ENST00000513671.5:c.-11-58633T>C	ENSP00000426739.1:n.-11-58633T>C
ENST00000615111.4:c.-296-6849T>C	ENSP00000478291.1:n.-296-6849T>C
ENST00000620156.4:c.11-58633T>C	ENSP00000483403.1:n.11-58633T>C
NM_000163.4:c.-11-58633T>C	NP_000154.1:n.-11-58633T>C
NM_001242399.2:c.11-58633T>C	NP_001229328.1:n.11-58633T>C
NM_001242400.2:c.-296-6849T>C	NP_001229329.1:n.-296-6849T>C
NM_001242401.3:c.-12+23902T>C	NP_001229330.1:n.-12+23902T>C
XM_011514031.1:c.11-58633T>C	XP_011512333.1:n.11-58633T>C
NM_000163.5:c.-11-58633T>C MANE Select	NP_000154.1:n.-11-58633T>C
NM_001242401.4:c.-12+23902T>C	NP_001229330.1:n.-12+23902T>C