Canonical Allele Identifier: CA1846870587

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429811A= , CM000671.2:g.37429811A=	GRCh38
NC_000009.11:g.37429808A= , CM000671.1:g.37429808A=	GRCh37
NC_000009.10:g.37419808A=	NCBI36
NG_008135.1:g.12102A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.573A= MANE Select	ENSP00000313432.6:p.Glu191=
ENST00000318158.10:c.573A=	ENSP00000313432.6:p.Glu191=
ENST00000377824.8:n.610A=
ENST00000460882.5:n.600A=
ENST00000480596.5:n.1274A=
ENST00000482603.1:n.26A=
ENST00000491488.5:n.278A=
ENST00000494290.1:c.144A=	ENSP00000432021.1:p.Glu48=
ENST00000497693.1:n.2106A=
ENST00000607784.1:c.573A=	ENSP00000475569.1:p.Glu191=
NM_012203.1:c.573A=	NP_036335.1:p.Glu191=
XM_005251631.1:c.252A=	XP_005251688.1:p.Glu84=
XM_011518073.1:c.171A=	XP_011516375.1:p.Glu57=
XR_929374.1:n.1018A=
XM_017015320.2:c.573A=	XP_016870809.1:p.Glu191=
XM_017015321.2:c.573A=	XP_016870810.1:p.Glu191=
XM_017015323.2:c.171A=	XP_016870812.1:p.Glu57=
XM_024447716.1:c.846A=	XP_024303484.1:p.Glu282=
XM_024447717.1:c.846A=	XP_024303485.1:p.Glu282=
XR_002956828.1:n.861A=
XR_002956829.1:n.861A=
XR_002956830.1:n.632A=
XR_002956831.1:n.307A=
XR_002956832.1:n.992A=
NM_012203.2:c.573A= MANE Select	NP_036335.1:p.Glu191=