Canonical Allele Identifier: CA1846886750

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436848T= , CM000671.2:g.37436848T=	GRCh38
NC_000009.11:g.37436845T= , CM000671.1:g.37436845T=	GRCh37
NC_000009.10:g.37426845T=	NCBI36
NG_008135.1:g.19139T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.*66T= MANE Select	ENSP00000313432.6:n.*66T=
ENST00000318158.10:c.*66T=	ENSP00000313432.6:n.*66T=
ENST00000460882.5:n.1080T=
ENST00000480596.5:n.1754T=
ENST00000494290.1:c.*52-33T=	ENSP00000432021.1:n.*52-33T=
ENST00000497693.1:n.4621T=
NM_012203.1:c.*66T=	NP_036335.1:n.*66T=
XM_005251631.1:c.*66T=	XP_005251688.1:n.*66T=
XM_011518073.1:c.*66T=	XP_011516375.1:n.*66T=
XM_017015320.2:c.946-563T=	XP_016870809.1:n.946-563T=
XM_017015321.2:c.866-563T=	XP_016870810.1:n.866-563T=
XM_017015323.2:c.544-563T=	XP_016870812.1:n.544-563T=
XM_024447716.1:c.1219-563T=	XP_024303484.1:n.1219-563T=
XM_024447717.1:c.1139-563T=	XP_024303485.1:n.1139-563T=
XR_002956828.1:n.1234-563T=
XR_002956829.1:n.1154-563T=
XR_002956830.1:n.2473T=
XR_002956831.1:n.2148T=
XR_002956832.1:n.1472T=
NM_012203.2:c.*66T= MANE Select	NP_036335.1:n.*66T=