Canonical Allele Identifier: CA1846873884

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37432013A= , CM000671.2:g.37432013A=	GRCh38
NC_000009.11:g.37432010A= , CM000671.1:g.37432010A=	GRCh37
NC_000009.10:g.37422010A=	NCBI36
NG_008135.1:g.14304A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.740A= MANE Select	ENSP00000313432.6:p.Asp247=
ENST00000318158.10:c.740A=	ENSP00000313432.6:p.Asp247=
ENST00000460882.5:n.767A=
ENST00000480596.5:n.1441A=
ENST00000482603.1:n.193A=
ENST00000491488.5:n.445A=
ENST00000494290.1:c.*51+862A=	ENSP00000432021.1:n.*51+862A=
ENST00000497693.1:n.4308A=
ENST00000607784.1:c.740A=	ENSP00000475569.1:p.Asp247=
NM_012203.1:c.740A=	NP_036335.1:p.Asp247=
XM_005251631.1:c.419A=	XP_005251688.1:p.Asp140=
XM_011518073.1:c.338A=	XP_011516375.1:p.Asp113=
XM_017015320.2:c.740A=	XP_016870809.1:p.Asp247=
XM_017015321.2:c.740A=	XP_016870810.1:p.Asp247=
XM_017015323.2:c.338A=	XP_016870812.1:p.Asp113=
XM_024447716.1:c.1013A=	XP_024303484.1:p.Asp338=
XM_024447717.1:c.1013A=	XP_024303485.1:p.Asp338=
XR_002956828.1:n.1028A=
XR_002956829.1:n.1028A=
XR_002956830.1:n.2160A=
XR_002956831.1:n.1835A=
XR_002956832.1:n.1159A=
NM_012203.2:c.740A= MANE Select	NP_036335.1:p.Asp247=