Canonical Allele Identifier: CA373443505

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37429812G>A (hg19) ; chr9:g.37429815G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429815G>A , CM000671.2:g.37429815G>A	GRCh38
NC_000009.11:g.37429812G>A , CM000671.1:g.37429812G>A	GRCh37
NC_000009.10:g.37419812G>A	NCBI36
NG_008135.1:g.12106G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.577G>A MANE Select	ENSP00000313432.6:p.Ala193Thr
ENST00000318158.10:c.577G>A	ENSP00000313432.6:p.Ala193Thr
ENST00000377824.8:n.614G>A
ENST00000460882.5:n.604G>A
ENST00000480596.5:n.1278G>A
ENST00000482603.1:n.30G>A
ENST00000491488.5:n.282G>A
ENST00000494290.1:c.148G>A	ENSP00000432021.1:p.Ala50Thr
ENST00000497693.1:n.2110G>A
ENST00000607784.1:c.577G>A	ENSP00000475569.1:p.Ala193Thr
NM_012203.1:c.577G>A	NP_036335.1:p.Ala193Thr
XM_005251631.1:c.256G>A	XP_005251688.1:p.Ala86Thr
XM_011518073.1:c.175G>A	XP_011516375.1:p.Ala59Thr
XR_929374.1:n.1022G>A
XM_017015320.2:c.577G>A	XP_016870809.1:p.Ala193Thr
XM_017015321.2:c.577G>A	XP_016870810.1:p.Ala193Thr
XM_017015323.2:c.175G>A	XP_016870812.1:p.Ala59Thr
XM_024447716.1:c.850G>A	XP_024303484.1:p.Ala284Thr
XM_024447717.1:c.850G>A	XP_024303485.1:p.Ala284Thr
XR_002956828.1:n.865G>A
XR_002956829.1:n.865G>A
XR_002956830.1:n.636G>A
XR_002956831.1:n.311G>A
XR_002956832.1:n.996G>A
NM_012203.2:c.577G>A MANE Select	NP_036335.1:p.Ala193Thr