Canonical Allele Identifier: CA1846886072

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436786A= , CM000671.2:g.37436786A=	GRCh38
NC_000009.11:g.37436783A= , CM000671.1:g.37436783A=	GRCh37
NC_000009.10:g.37426783A=	NCBI36
NG_008135.1:g.19077A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*4A= MANE Select	ENSP00000313432.6:n.*4A=
ENST00000318158.10:c.*4A=	ENSP00000313432.6:n.*4A=
ENST00000460882.5:n.1018A=
ENST00000480596.5:n.1692A=
ENST00000494290.1:c.*52-95A=	ENSP00000432021.1:n.*52-95A=
ENST00000497693.1:n.4559A=
NM_012203.1:c.*4A=	NP_036335.1:n.*4A=
XM_005251631.1:c.*4A=	XP_005251688.1:n.*4A=
XM_011518073.1:c.*4A=	XP_011516375.1:n.*4A=
XM_017015320.2:c.946-625A=	XP_016870809.1:n.946-625A=
XM_017015321.2:c.866-625A=	XP_016870810.1:n.866-625A=
XM_017015323.2:c.544-625A=	XP_016870812.1:n.544-625A=
XM_024447716.1:c.1219-625A=	XP_024303484.1:n.1219-625A=
XM_024447717.1:c.1139-625A=	XP_024303485.1:n.1139-625A=
XR_002956828.1:n.1234-625A=
XR_002956829.1:n.1154-625A=
XR_002956830.1:n.2411A=
XR_002956831.1:n.2086A=
XR_002956832.1:n.1410A=
NM_012203.2:c.*4A= MANE Select	NP_036335.1:n.*4A=