Canonical Allele Identifier: CA1846874339

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37432134_37432136delinsCTG , CM000671.2:g.37432134_37432136delinsCTG	GRCh38
NC_000009.11:g.37432131_37432133delinsCTG , CM000671.1:g.37432131_37432133delinsCTG	GRCh37
NC_000009.10:g.37422131_37422133delinsCTG	NCBI36
NG_008135.1:g.14425_14427delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.861_863delinsCTG MANE Select	ENSP00000313432.6:p.Asn287=
ENST00000318158.10:c.861_863delinsCTG	ENSP00000313432.6:p.Asn287=
ENST00000460882.5:n.888_890delinsCTG
ENST00000480596.5:n.1562_1564delinsCTG
ENST00000482603.1:n.314_316delinsCTG
ENST00000491488.5:n.566_568delinsCTG
ENST00000494290.1:c.*51+983_*51+985delinsCTG	ENSP00000432021.1:n.*51+983_*51+985delinsCTG
ENST00000497693.1:n.4429_4431delinsCTG
ENST00000512404.2:n.48_50delinsCTG
ENST00000607784.1:c.861_863delinsCTG	ENSP00000475569.1:p.Asn287=
NM_012203.1:c.861_863delinsCTG	NP_036335.1:p.Asn287=
XM_005251631.1:c.540_542delinsCTG	XP_005251688.1:p.Asn180=
XM_011518073.1:c.459_461delinsCTG	XP_011516375.1:p.Asn153=
XM_017015320.2:c.861_863delinsCTG	XP_016870809.1:p.Asn287=
XM_017015321.2:c.861_863delinsCTG	XP_016870810.1:p.Asn287=
XM_017015323.2:c.459_461delinsCTG	XP_016870812.1:p.Asn153=
XM_024447716.1:c.1134_1136delinsCTG	XP_024303484.1:p.Asn378=
XM_024447717.1:c.1134_1136delinsCTG	XP_024303485.1:p.Asn378=
XR_002956828.1:n.1149_1151delinsCTG
XR_002956829.1:n.1149_1151delinsCTG
XR_002956830.1:n.2281_2283delinsCTG
XR_002956831.1:n.1956_1958delinsCTG
XR_002956832.1:n.1280_1282delinsCTG
NM_012203.2:c.861_863delinsCTG MANE Select	NP_036335.1:p.Asn287=