Canonical Allele Identifier: CA1846870564

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429800A= , CM000671.2:g.37429800A=	GRCh38
NC_000009.11:g.37429797A= , CM000671.1:g.37429797A=	GRCh37
NC_000009.10:g.37419797A=	NCBI36
NG_008135.1:g.12091A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.562A= MANE Select	ENSP00000313432.6:p.Arg188=
ENST00000318158.10:c.562A=	ENSP00000313432.6:p.Arg188=
ENST00000377824.8:n.599A=
ENST00000460882.5:n.589A=
ENST00000480596.5:n.1263A=
ENST00000482603.1:n.15A=
ENST00000491488.5:n.267A=
ENST00000494290.1:c.133A=	ENSP00000432021.1:p.Arg45=
ENST00000497693.1:n.2095A=
ENST00000607784.1:c.562A=	ENSP00000475569.1:p.Arg188=
NM_012203.1:c.562A=	NP_036335.1:p.Arg188=
XM_005251631.1:c.241A=	XP_005251688.1:p.Arg81=
XM_011518073.1:c.160A=	XP_011516375.1:p.Arg54=
XR_929374.1:n.1007A=
XM_017015320.2:c.562A=	XP_016870809.1:p.Arg188=
XM_017015321.2:c.562A=	XP_016870810.1:p.Arg188=
XM_017015323.2:c.160A=	XP_016870812.1:p.Arg54=
XM_024447716.1:c.835A=	XP_024303484.1:p.Arg279=
XM_024447717.1:c.835A=	XP_024303485.1:p.Arg279=
XR_002956828.1:n.850A=
XR_002956829.1:n.850A=
XR_002956830.1:n.621A=
XR_002956831.1:n.296A=
XR_002956832.1:n.981A=
NM_012203.2:c.562A= MANE Select	NP_036335.1:p.Arg188=