Canonical Allele Identifier: CA1846870454

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429739C= , CM000671.2:g.37429739C=	GRCh38
NC_000009.11:g.37429736C= , CM000671.1:g.37429736C=	GRCh37
NC_000009.10:g.37419736C=	NCBI36
NG_008135.1:g.12030C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.501C= MANE Select	ENSP00000313432.6:p.Ala167=
ENST00000318158.10:c.501C=	ENSP00000313432.6:p.Ala167=
ENST00000377824.8:n.538C=
ENST00000460882.5:n.528C=
ENST00000480596.5:n.1202C=
ENST00000491488.5:n.206C=
ENST00000494290.1:c.72C=	ENSP00000432021.1:p.Ala24=
ENST00000497693.1:n.2034C=
ENST00000607784.1:c.501C=	ENSP00000475569.1:p.Ala167=
NM_012203.1:c.501C=	NP_036335.1:p.Ala167=
XM_005251631.1:c.180C=	XP_005251688.1:p.Ala60=
XM_011518073.1:c.99C=	XP_011516375.1:p.Ala33=
XR_929374.1:n.946C=
XM_017015320.2:c.501C=	XP_016870809.1:p.Ala167=
XM_017015321.2:c.501C=	XP_016870810.1:p.Ala167=
XM_017015323.2:c.99C=	XP_016870812.1:p.Ala33=
XM_024447716.1:c.774C=	XP_024303484.1:p.Ala258=
XM_024447717.1:c.774C=	XP_024303485.1:p.Ala258=
XR_002956828.1:n.789C=
XR_002956829.1:n.789C=
XR_002956830.1:n.560C=
XR_002956831.1:n.235C=
XR_002956832.1:n.920C=
NM_012203.2:c.501C= MANE Select	NP_036335.1:p.Ala167=