Canonical Allele Identifier: CA1846870523

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429775_37429776delinsAT , CM000671.2:g.37429775_37429776delinsAT	GRCh38
NC_000009.11:g.37429772_37429773delinsAT , CM000671.1:g.37429772_37429773delinsAT	GRCh37
NC_000009.10:g.37419772_37419773delinsAT	NCBI36
NG_008135.1:g.12066_12067delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.537_538delinsAT MANE Select	ENSP00000313432.6:p.Arg179=
ENST00000318158.10:c.537_538delinsAT	ENSP00000313432.6:p.Arg179=
ENST00000377824.8:n.574_575delinsAT
ENST00000460882.5:n.564_565delinsAT
ENST00000480596.5:n.1238_1239delinsAT
ENST00000491488.5:n.242_243delinsAT
ENST00000494290.1:c.108_109delinsAT	ENSP00000432021.1:p.Arg36=
ENST00000497693.1:n.2070_2071delinsAT
ENST00000607784.1:c.537_538delinsAT	ENSP00000475569.1:p.Arg179=
NM_012203.1:c.537_538delinsAT	NP_036335.1:p.Arg179=
XM_005251631.1:c.216_217delinsAT	XP_005251688.1:p.Arg72=
XM_011518073.1:c.135_136delinsAT	XP_011516375.1:p.Arg45=
XR_929374.1:n.982_983delinsAT
XM_017015320.2:c.537_538delinsAT	XP_016870809.1:p.Arg179=
XM_017015321.2:c.537_538delinsAT	XP_016870810.1:p.Arg179=
XM_017015323.2:c.135_136delinsAT	XP_016870812.1:p.Arg45=
XM_024447716.1:c.810_811delinsAT	XP_024303484.1:p.Arg270=
XM_024447717.1:c.810_811delinsAT	XP_024303485.1:p.Arg270=
XR_002956828.1:n.825_826delinsAT
XR_002956829.1:n.825_826delinsAT
XR_002956830.1:n.596_597delinsAT
XR_002956831.1:n.271_272delinsAT
XR_002956832.1:n.956_957delinsAT
NM_012203.2:c.537_538delinsAT MANE Select	NP_036335.1:p.Arg179=