Canonical Allele Identifier: CA1846874349

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37432135_37432136delinsTG , CM000671.2:g.37432135_37432136delinsTG	GRCh38
NC_000009.11:g.37432132_37432133delinsTG , CM000671.1:g.37432132_37432133delinsTG	GRCh37
NC_000009.10:g.37422132_37422133delinsTG	NCBI36
NG_008135.1:g.14426_14427delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.862_863delinsTG MANE Select	ENSP00000313432.6:p.Cys288=
ENST00000318158.10:c.862_863delinsTG	ENSP00000313432.6:p.Cys288=
ENST00000460882.5:n.889_890delinsTG
ENST00000480596.5:n.1563_1564delinsTG
ENST00000482603.1:n.315_316delinsTG
ENST00000491488.5:n.567_568delinsTG
ENST00000494290.1:c.*51+984_*51+985delinsTG	ENSP00000432021.1:n.*51+984_*51+985delinsTG
ENST00000497693.1:n.4430_4431delinsTG
ENST00000512404.2:n.49_50delinsTG
ENST00000607784.1:c.862_863delinsTG	ENSP00000475569.1:p.Cys288=
NM_012203.1:c.862_863delinsTG	NP_036335.1:p.Cys288=
XM_005251631.1:c.541_542delinsTG	XP_005251688.1:p.Cys181=
XM_011518073.1:c.460_461delinsTG	XP_011516375.1:p.Cys154=
XM_017015320.2:c.862_863delinsTG	XP_016870809.1:p.Cys288=
XM_017015321.2:c.862_863delinsTG	XP_016870810.1:p.Cys288=
XM_017015323.2:c.460_461delinsTG	XP_016870812.1:p.Cys154=
XM_024447716.1:c.1135_1136delinsTG	XP_024303484.1:p.Cys379=
XM_024447717.1:c.1135_1136delinsTG	XP_024303485.1:p.Cys379=
XR_002956828.1:n.1150_1151delinsTG
XR_002956829.1:n.1150_1151delinsTG
XR_002956830.1:n.2282_2283delinsTG
XR_002956831.1:n.1957_1958delinsTG
XR_002956832.1:n.1281_1282delinsTG
NM_012203.2:c.862_863delinsTG MANE Select	NP_036335.1:p.Cys288=