Canonical Allele Identifier: CA1846870449

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429737G= , CM000671.2:g.37429737G=	GRCh38
NC_000009.11:g.37429734G= , CM000671.1:g.37429734G=	GRCh37
NC_000009.10:g.37419734G=	NCBI36
NG_008135.1:g.12028G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.499G= MANE Select	ENSP00000313432.6:p.Ala167=
ENST00000318158.10:c.499G=	ENSP00000313432.6:p.Ala167=
ENST00000377824.8:n.536G=
ENST00000460882.5:n.526G=
ENST00000480596.5:n.1200G=
ENST00000491488.5:n.204G=
ENST00000494290.1:c.70G=	ENSP00000432021.1:p.Ala24=
ENST00000497693.1:n.2032G=
ENST00000607784.1:c.499G=	ENSP00000475569.1:p.Ala167=
NM_012203.1:c.499G=	NP_036335.1:p.Ala167=
XM_005251631.1:c.178G=	XP_005251688.1:p.Ala60=
XM_011518073.1:c.97G=	XP_011516375.1:p.Ala33=
XR_929374.1:n.944G=
XM_017015320.2:c.499G=	XP_016870809.1:p.Ala167=
XM_017015321.2:c.499G=	XP_016870810.1:p.Ala167=
XM_017015323.2:c.97G=	XP_016870812.1:p.Ala33=
XM_024447716.1:c.772G=	XP_024303484.1:p.Ala258=
XM_024447717.1:c.772G=	XP_024303485.1:p.Ala258=
XR_002956828.1:n.787G=
XR_002956829.1:n.787G=
XR_002956830.1:n.558G=
XR_002956831.1:n.233G=
XR_002956832.1:n.918G=
NM_012203.2:c.499G= MANE Select	NP_036335.1:p.Ala167=