Canonical Allele Identifier: CA1846870602

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429821T= , CM000671.2:g.37429821T=	GRCh38
NC_000009.11:g.37429818T= , CM000671.1:g.37429818T=	GRCh37
NC_000009.10:g.37419818T=	NCBI36
NG_008135.1:g.12112T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.583T= MANE Select	ENSP00000313432.6:p.Phe195=
ENST00000318158.10:c.583T=	ENSP00000313432.6:p.Phe195=
ENST00000377824.8:n.620T=
ENST00000460882.5:n.610T=
ENST00000480596.5:n.1284T=
ENST00000482603.1:n.36T=
ENST00000491488.5:n.288T=
ENST00000494290.1:c.154T=	ENSP00000432021.1:p.Phe52=
ENST00000497693.1:n.2116T=
ENST00000607784.1:c.583T=	ENSP00000475569.1:p.Phe195=
NM_012203.1:c.583T=	NP_036335.1:p.Phe195=
XM_005251631.1:c.262T=	XP_005251688.1:p.Phe88=
XM_011518073.1:c.181T=	XP_011516375.1:p.Phe61=
XR_929374.1:n.1028T=
XM_017015320.2:c.583T=	XP_016870809.1:p.Phe195=
XM_017015321.2:c.583T=	XP_016870810.1:p.Phe195=
XM_017015323.2:c.181T=	XP_016870812.1:p.Phe61=
XM_024447716.1:c.856T=	XP_024303484.1:p.Phe286=
XM_024447717.1:c.856T=	XP_024303485.1:p.Phe286=
XR_002956828.1:n.871T=
XR_002956829.1:n.871T=
XR_002956830.1:n.642T=
XR_002956831.1:n.317T=
XR_002956832.1:n.1002T=
NM_012203.2:c.583T= MANE Select	NP_036335.1:p.Phe195=