Canonical Allele Identifier: CA5058890

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37422784A>G , CM000671.2:g.37422784A>G	GRCh38
NC_000009.11:g.37422781A>G , CM000671.1:g.37422781A>G	GRCh37
NC_000009.10:g.37412781A>G	NCBI36
NG_008135.1:g.5075A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_012203.2:c.34A>G MANE Select	NP_036335.1:p.Thr12Ala
ENST00000318158.11:c.34A>G MANE Select	ENSP00000313432.6:p.Thr12Ala
NM_012203.1:c.34A>G	NP_036335.1:p.Thr12Ala
ENST00000318158.10:c.34A>G	ENSP00000313432.6:p.Thr12Ala
ENST00000377824.8:n.71A>G
ENST00000460882.5:n.89A>G
ENST00000487399.5:n.71A>G
ENST00000491488.5:n.60A>G
ENST00000493368.5:n.119A>G
ENST00000607784.1:c.34A>G	ENSP00000475569.1:p.Thr12Ala
XM_005251631.1:c.34A>G	XP_005251688.1:p.Thr12Ala
XM_011518073.1:c.-729A>G	XP_011516375.1:n.-729A>G
XM_017015320.2:c.34A>G	XP_016870809.1:p.Thr12Ala
XM_017015321.2:c.34A>G	XP_016870810.1:p.Thr12Ala
XM_017015323.2:c.-729A>G	XP_016870812.1:n.-729A>G
XM_024447716.1:c.335A>G	XP_024303484.1:p.His112Arg
XM_024447717.1:c.335A>G	XP_024303485.1:p.His112Arg
XR_002956828.1:n.350A>G
XR_002956829.1:n.350A>G
XR_002956830.1:n.93A>G
XR_002956831.1:n.89A>G
XR_002956832.1:n.93A>G
XR_929374.1:n.119A>G