Canonical Allele Identifier: CA1846873817

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37432007G= , CM000671.2:g.37432007G=	GRCh38
NC_000009.11:g.37432004G= , CM000671.1:g.37432004G=	GRCh37
NC_000009.10:g.37422004G=	NCBI36
NG_008135.1:g.14298G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.735-1G= MANE Select	ENSP00000313432.6:n.735-1G=
ENST00000318158.10:c.735-1G=	ENSP00000313432.6:n.735-1G=
ENST00000460882.5:n.762-1G=
ENST00000480596.5:n.1436-1G=
ENST00000482603.1:n.188-1G=
ENST00000491488.5:n.440-1G=
ENST00000494290.1:c.*51+856G=	ENSP00000432021.1:n.*51+856G=
ENST00000497693.1:n.4302G=
ENST00000607784.1:c.735-1G=	ENSP00000475569.1:n.735-1G=
NM_012203.1:c.735-1G=	NP_036335.1:n.735-1G=
XM_005251631.1:c.414-1G=	XP_005251688.1:n.414-1G=
XM_011518073.1:c.333-1G=	XP_011516375.1:n.333-1G=
XM_017015320.2:c.735-1G=	XP_016870809.1:n.735-1G=
XM_017015321.2:c.735-1G=	XP_016870810.1:n.735-1G=
XM_017015323.2:c.333-1G=	XP_016870812.1:n.333-1G=
XM_024447716.1:c.1008-1G=	XP_024303484.1:n.1008-1G=
XM_024447717.1:c.1008-1G=	XP_024303485.1:n.1008-1G=
XR_002956828.1:n.1023-1G=
XR_002956829.1:n.1023-1G=
XR_002956830.1:n.2154G=
XR_002956831.1:n.1829G=
XR_002956832.1:n.1154-1G=
NM_012203.2:c.735-1G= MANE Select	NP_036335.1:n.735-1G=