Canonical Allele Identifier: CA1846870448

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429737_37429738delinsGC , CM000671.2:g.37429737_37429738delinsGC	GRCh38
NC_000009.11:g.37429734_37429735delinsGC , CM000671.1:g.37429734_37429735delinsGC	GRCh37
NC_000009.10:g.37419734_37419735delinsGC	NCBI36
NG_008135.1:g.12028_12029delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.499_500delinsGC MANE Select	ENSP00000313432.6:p.Ala167=
ENST00000318158.10:c.499_500delinsGC	ENSP00000313432.6:p.Ala167=
ENST00000377824.8:n.536_537delinsGC
ENST00000460882.5:n.526_527delinsGC
ENST00000480596.5:n.1200_1201delinsGC
ENST00000491488.5:n.204_205delinsGC
ENST00000494290.1:c.70_71delinsGC	ENSP00000432021.1:p.Ala24=
ENST00000497693.1:n.2032_2033delinsGC
ENST00000607784.1:c.499_500delinsGC	ENSP00000475569.1:p.Ala167=
NM_012203.1:c.499_500delinsGC	NP_036335.1:p.Ala167=
XM_005251631.1:c.178_179delinsGC	XP_005251688.1:p.Ala60=
XM_011518073.1:c.97_98delinsGC	XP_011516375.1:p.Ala33=
XR_929374.1:n.944_945delinsGC
XM_017015320.2:c.499_500delinsGC	XP_016870809.1:p.Ala167=
XM_017015321.2:c.499_500delinsGC	XP_016870810.1:p.Ala167=
XM_017015323.2:c.97_98delinsGC	XP_016870812.1:p.Ala33=
XM_024447716.1:c.772_773delinsGC	XP_024303484.1:p.Ala258=
XM_024447717.1:c.772_773delinsGC	XP_024303485.1:p.Ala258=
XR_002956828.1:n.787_788delinsGC
XR_002956829.1:n.787_788delinsGC
XR_002956830.1:n.558_559delinsGC
XR_002956831.1:n.233_234delinsGC
XR_002956832.1:n.918_919delinsGC
NM_012203.2:c.499_500delinsGC MANE Select	NP_036335.1:p.Ala167=