Canonical Allele Identifier: CA1846870439

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429732_37429733delinsGC , CM000671.2:g.37429732_37429733delinsGC	GRCh38
NC_000009.11:g.37429729_37429730delinsGC , CM000671.1:g.37429729_37429730delinsGC	GRCh37
NC_000009.10:g.37419729_37419730delinsGC	NCBI36
NG_008135.1:g.12023_12024delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.494_495delinsGC MANE Select	ENSP00000313432.6:p.Gly165=
ENST00000318158.10:c.494_495delinsGC	ENSP00000313432.6:p.Gly165=
ENST00000377824.8:n.531_532delinsGC
ENST00000460882.5:n.521_522delinsGC
ENST00000480596.5:n.1195_1196delinsGC
ENST00000491488.5:n.199_200delinsGC
ENST00000494290.1:c.65_66delinsGC	ENSP00000432021.1:p.Gly22=
ENST00000497693.1:n.2027_2028delinsGC
ENST00000607784.1:c.494_495delinsGC	ENSP00000475569.1:p.Gly165=
NM_012203.1:c.494_495delinsGC	NP_036335.1:p.Gly165=
XM_005251631.1:c.173_174delinsGC	XP_005251688.1:p.Gly58=
XM_011518073.1:c.92_93delinsGC	XP_011516375.1:p.Gly31=
XR_929374.1:n.939_940delinsGC
XM_017015320.2:c.494_495delinsGC	XP_016870809.1:p.Gly165=
XM_017015321.2:c.494_495delinsGC	XP_016870810.1:p.Gly165=
XM_017015323.2:c.92_93delinsGC	XP_016870812.1:p.Gly31=
XM_024447716.1:c.767_768delinsGC	XP_024303484.1:p.Gly256=
XM_024447717.1:c.767_768delinsGC	XP_024303485.1:p.Gly256=
XR_002956828.1:n.782_783delinsGC
XR_002956829.1:n.782_783delinsGC
XR_002956830.1:n.553_554delinsGC
XR_002956831.1:n.228_229delinsGC
XR_002956832.1:n.913_914delinsGC
NM_012203.2:c.494_495delinsGC MANE Select	NP_036335.1:p.Gly165=