Canonical Allele Identifier: CA1846874331

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37432132A= , CM000671.2:g.37432132A=	GRCh38
NC_000009.11:g.37432129A= , CM000671.1:g.37432129A=	GRCh37
NC_000009.10:g.37422129A=	NCBI36
NG_008135.1:g.14423A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.859A= MANE Select	ENSP00000313432.6:p.Asn287=
ENST00000318158.10:c.859A=	ENSP00000313432.6:p.Asn287=
ENST00000460882.5:n.886A=
ENST00000480596.5:n.1560A=
ENST00000482603.1:n.312A=
ENST00000491488.5:n.564A=
ENST00000494290.1:c.*51+981A=	ENSP00000432021.1:n.*51+981A=
ENST00000497693.1:n.4427A=
ENST00000512404.2:n.46A=
ENST00000607784.1:c.859A=	ENSP00000475569.1:p.Asn287=
NM_012203.1:c.859A=	NP_036335.1:p.Asn287=
XM_005251631.1:c.538A=	XP_005251688.1:p.Asn180=
XM_011518073.1:c.457A=	XP_011516375.1:p.Asn153=
XM_017015320.2:c.859A=	XP_016870809.1:p.Asn287=
XM_017015321.2:c.859A=	XP_016870810.1:p.Asn287=
XM_017015323.2:c.457A=	XP_016870812.1:p.Asn153=
XM_024447716.1:c.1132A=	XP_024303484.1:p.Asn378=
XM_024447717.1:c.1132A=	XP_024303485.1:p.Asn378=
XR_002956828.1:n.1147A=
XR_002956829.1:n.1147A=
XR_002956830.1:n.2279A=
XR_002956831.1:n.1954A=
XR_002956832.1:n.1278A=
NM_012203.2:c.859A= MANE Select	NP_036335.1:p.Asn287=