Canonical Allele Identifier: CA1846870508

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429763C= , CM000671.2:g.37429763C=	GRCh38
NC_000009.11:g.37429760C= , CM000671.1:g.37429760C=	GRCh37
NC_000009.10:g.37419760C=	NCBI36
NG_008135.1:g.12054C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.525C= MANE Select	ENSP00000313432.6:p.Phe175=
ENST00000318158.10:c.525C=	ENSP00000313432.6:p.Phe175=
ENST00000377824.8:n.562C=
ENST00000460882.5:n.552C=
ENST00000480596.5:n.1226C=
ENST00000491488.5:n.230C=
ENST00000494290.1:c.96C=	ENSP00000432021.1:p.Phe32=
ENST00000497693.1:n.2058C=
ENST00000607784.1:c.525C=	ENSP00000475569.1:p.Phe175=
NM_012203.1:c.525C=	NP_036335.1:p.Phe175=
XM_005251631.1:c.204C=	XP_005251688.1:p.Phe68=
XM_011518073.1:c.123C=	XP_011516375.1:p.Phe41=
XR_929374.1:n.970C=
XM_017015320.2:c.525C=	XP_016870809.1:p.Phe175=
XM_017015321.2:c.525C=	XP_016870810.1:p.Phe175=
XM_017015323.2:c.123C=	XP_016870812.1:p.Phe41=
XM_024447716.1:c.798C=	XP_024303484.1:p.Phe266=
XM_024447717.1:c.798C=	XP_024303485.1:p.Phe266=
XR_002956828.1:n.813C=
XR_002956829.1:n.813C=
XR_002956830.1:n.584C=
XR_002956831.1:n.259C=
XR_002956832.1:n.944C=
NM_012203.2:c.525C= MANE Select	NP_036335.1:p.Phe175=