Canonical Allele Identifier: CA1846870456

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429740A= , CM000671.2:g.37429740A=	GRCh38
NC_000009.11:g.37429737A= , CM000671.1:g.37429737A=	GRCh37
NC_000009.10:g.37419737A=	NCBI36
NG_008135.1:g.12031A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.502A= MANE Select	ENSP00000313432.6:p.Ile168=
ENST00000318158.10:c.502A=	ENSP00000313432.6:p.Ile168=
ENST00000377824.8:n.539A=
ENST00000460882.5:n.529A=
ENST00000480596.5:n.1203A=
ENST00000491488.5:n.207A=
ENST00000494290.1:c.73A=	ENSP00000432021.1:p.Ile25=
ENST00000497693.1:n.2035A=
ENST00000607784.1:c.502A=	ENSP00000475569.1:p.Ile168=
NM_012203.1:c.502A=	NP_036335.1:p.Ile168=
XM_005251631.1:c.181A=	XP_005251688.1:p.Ile61=
XM_011518073.1:c.100A=	XP_011516375.1:p.Ile34=
XR_929374.1:n.947A=
XM_017015320.2:c.502A=	XP_016870809.1:p.Ile168=
XM_017015321.2:c.502A=	XP_016870810.1:p.Ile168=
XM_017015323.2:c.100A=	XP_016870812.1:p.Ile34=
XM_024447716.1:c.775A=	XP_024303484.1:p.Ile259=
XM_024447717.1:c.775A=	XP_024303485.1:p.Ile259=
XR_002956828.1:n.790A=
XR_002956829.1:n.790A=
XR_002956830.1:n.561A=
XR_002956831.1:n.236A=
XR_002956832.1:n.921A=
NM_012203.2:c.502A= MANE Select	NP_036335.1:p.Ile168=