Canonical Allele Identifier: CA1846874005

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37432029C= , CM000671.2:g.37432029C=	GRCh38
NC_000009.11:g.37432026C= , CM000671.1:g.37432026C=	GRCh37
NC_000009.10:g.37422026C=	NCBI36
NG_008135.1:g.14320C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.756C= MANE Select	ENSP00000313432.6:p.Asp252=
ENST00000318158.10:c.756C=	ENSP00000313432.6:p.Asp252=
ENST00000460882.5:n.783C=
ENST00000480596.5:n.1457C=
ENST00000482603.1:n.209C=
ENST00000491488.5:n.461C=
ENST00000494290.1:c.*51+878C=	ENSP00000432021.1:n.*51+878C=
ENST00000497693.1:n.4324C=
ENST00000607784.1:c.756C=	ENSP00000475569.1:p.Asp252=
NM_012203.1:c.756C=	NP_036335.1:p.Asp252=
XM_005251631.1:c.435C=	XP_005251688.1:p.Asp145=
XM_011518073.1:c.354C=	XP_011516375.1:p.Asp118=
XM_017015320.2:c.756C=	XP_016870809.1:p.Asp252=
XM_017015321.2:c.756C=	XP_016870810.1:p.Asp252=
XM_017015323.2:c.354C=	XP_016870812.1:p.Asp118=
XM_024447716.1:c.1029C=	XP_024303484.1:p.Asp343=
XM_024447717.1:c.1029C=	XP_024303485.1:p.Asp343=
XR_002956828.1:n.1044C=
XR_002956829.1:n.1044C=
XR_002956830.1:n.2176C=
XR_002956831.1:n.1851C=
XR_002956832.1:n.1175C=
NM_012203.2:c.756C= MANE Select	NP_036335.1:p.Asp252=