Canonical Allele Identifier: CA1846870618

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429832_37429833delinsGT , CM000671.2:g.37429832_37429833delinsGT	GRCh38
NC_000009.11:g.37429829_37429830delinsGT , CM000671.1:g.37429829_37429830delinsGT	GRCh37
NC_000009.10:g.37419829_37419830delinsGT	NCBI36
NG_008135.1:g.12123_12124delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.594_595delinsGT MANE Select	ENSP00000313432.6:p.Glu198=
ENST00000318158.10:c.594_595delinsGT	ENSP00000313432.6:p.Glu198=
ENST00000377824.8:n.631_632delinsGT
ENST00000460882.5:n.621_622delinsGT
ENST00000480596.5:n.1295_1296delinsGT
ENST00000482603.1:n.47_48delinsGT
ENST00000491488.5:n.299_300delinsGT
ENST00000494290.1:c.165_166delinsGT	ENSP00000432021.1:p.Glu55=
ENST00000497693.1:n.2127_2128delinsGT
ENST00000607784.1:c.594_595delinsGT	ENSP00000475569.1:p.Glu198=
NM_012203.1:c.594_595delinsGT	NP_036335.1:p.Glu198=
XM_005251631.1:c.273_274delinsGT	XP_005251688.1:p.Glu91=
XM_011518073.1:c.192_193delinsGT	XP_011516375.1:p.Glu64=
XR_929374.1:n.1039_1040delinsGT
XM_017015320.2:c.594_595delinsGT	XP_016870809.1:p.Glu198=
XM_017015321.2:c.594_595delinsGT	XP_016870810.1:p.Glu198=
XM_017015323.2:c.192_193delinsGT	XP_016870812.1:p.Glu64=
XM_024447716.1:c.867_868delinsGT	XP_024303484.1:p.Glu289=
XM_024447717.1:c.867_868delinsGT	XP_024303485.1:p.Glu289=
XR_002956828.1:n.882_883delinsGT
XR_002956829.1:n.882_883delinsGT
XR_002956830.1:n.653_654delinsGT
XR_002956831.1:n.328_329delinsGT
XR_002956832.1:n.1013_1014delinsGT
NM_012203.2:c.594_595delinsGT MANE Select	NP_036335.1:p.Glu198=