Canonical Allele Identifier: CA1846887015

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436953A= , CM000671.2:g.37436953A=	GRCh38
NC_000009.11:g.37436950A= , CM000671.1:g.37436950A=	GRCh37
NC_000009.10:g.37426950A=	NCBI36
NG_008135.1:g.19244A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*171A= MANE Select	ENSP00000313432.6:n.*171A=
ENST00000318158.10:c.*171A=	ENSP00000313432.6:n.*171A=
ENST00000480596.5:n.1859A=
ENST00000494290.1:c.*124A=	ENSP00000432021.1:n.*124A=
ENST00000497693.1:n.4726A=
NM_012203.1:c.*171A=	NP_036335.1:n.*171A=
XM_005251631.1:c.*171A=	XP_005251688.1:n.*171A=
XM_011518073.1:c.*171A=	XP_011516375.1:n.*171A=
XM_017015320.2:c.946-458A=	XP_016870809.1:n.946-458A=
XM_017015321.2:c.866-458A=	XP_016870810.1:n.866-458A=
XM_017015323.2:c.544-458A=	XP_016870812.1:n.544-458A=
XM_024447716.1:c.1219-458A=	XP_024303484.1:n.1219-458A=
XM_024447717.1:c.1139-458A=	XP_024303485.1:n.1139-458A=
XR_002956828.1:n.1234-458A=
XR_002956829.1:n.1154-458A=
XR_002956830.1:n.2578A=
XR_002956831.1:n.2253A=
XR_002956832.1:n.1577A=
NM_012203.2:c.*171A= MANE Select	NP_036335.1:n.*171A=