Canonical Allele Identifier: CA1846885990

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436768G= , CM000671.2:g.37436768G=	GRCh38
NC_000009.11:g.37436765G= , CM000671.1:g.37436765G=	GRCh37
NC_000009.10:g.37426765G=	NCBI36
NG_008135.1:g.19059G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.973G= MANE Select	ENSP00000313432.6:p.Glu325=
ENST00000318158.10:c.973G=	ENSP00000313432.6:p.Glu325=
ENST00000460882.5:n.1000G=
ENST00000480596.5:n.1674G=
ENST00000494290.1:c.*52-113G=	ENSP00000432021.1:n.*52-113G=
ENST00000497693.1:n.4541G=
NM_012203.1:c.973G=	NP_036335.1:p.Glu325=
XM_005251631.1:c.652G=	XP_005251688.1:p.Glu218=
XM_011518073.1:c.571G=	XP_011516375.1:p.Glu191=
XM_017015320.2:c.946-643G=	XP_016870809.1:n.946-643G=
XM_017015321.2:c.866-643G=	XP_016870810.1:n.866-643G=
XM_017015323.2:c.544-643G=	XP_016870812.1:n.544-643G=
XM_024447716.1:c.1219-643G=	XP_024303484.1:n.1219-643G=
XM_024447717.1:c.1139-643G=	XP_024303485.1:n.1139-643G=
XR_002956828.1:n.1234-643G=
XR_002956829.1:n.1154-643G=
XR_002956830.1:n.2393G=
XR_002956831.1:n.2068G=
XR_002956832.1:n.1392G=
NM_012203.2:c.973G= MANE Select	NP_036335.1:p.Glu325=