Canonical Allele Identifier: CA1846871130

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37430483T= , CM000671.2:g.37430483T=	GRCh38
NC_000009.11:g.37430480T= , CM000671.1:g.37430480T=	GRCh37
NC_000009.10:g.37420480T=	NCBI36
NG_008135.1:g.12774T=

Transcript Alleles

HGVS	Amino-acid Change
NM_012203.2:c.599-28T= MANE Select	NP_036335.1:n.599-28T=
ENST00000318158.11:c.599-28T= MANE Select	ENSP00000313432.6:n.599-28T=
NM_012203.1:c.599-28T=	NP_036335.1:n.599-28T=
ENST00000318158.10:c.599-28T=	ENSP00000313432.6:n.599-28T=
ENST00000377824.8:n.636-28T=
ENST00000460882.5:n.626-28T=
ENST00000480596.5:n.1300-28T=
ENST00000482603.1:n.52-28T=
ENST00000491488.5:n.304-28T=
ENST00000494290.1:c.170-28T=	ENSP00000432021.1:n.170-28T=
ENST00000497693.1:n.2778T=
ENST00000607784.1:c.599-28T=	ENSP00000475569.1:n.599-28T=
XM_005251631.1:c.278-28T=	XP_005251688.1:n.278-28T=
XM_011518073.1:c.197-28T=	XP_011516375.1:n.197-28T=
XM_017015320.2:c.599-28T=	XP_016870809.1:n.599-28T=
XM_017015321.2:c.599-28T=	XP_016870810.1:n.599-28T=
XM_017015323.2:c.197-28T=	XP_016870812.1:n.197-28T=
XM_024447716.1:c.872-28T=	XP_024303484.1:n.872-28T=
XM_024447717.1:c.872-28T=	XP_024303485.1:n.872-28T=
XR_002956828.1:n.887-28T=
XR_002956829.1:n.887-28T=
XR_002956830.1:n.658-28T=
XR_002956831.1:n.333-28T=
XR_002956832.1:n.1018-28T=
XR_929374.1:n.1044-28T=