Canonical Allele Identifier: CA373442610

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37426630A>T (hg19) ; chr9:g.37426633A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37426633A>T , CM000671.2:g.37426633A>T	GRCh38
NC_000009.11:g.37426630A>T , CM000671.1:g.37426630A>T	GRCh37
NC_000009.10:g.37416630A>T	NCBI36
NG_008135.1:g.8924A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000318158.11:c.383A>T MANE Select	ENSP00000313432.6:p.Glu128Val
ENST00000318158.10:c.383A>T	ENSP00000313432.6:p.Glu128Val
ENST00000377824.8:n.420A>T
ENST00000460882.5:n.410A>T
ENST00000487399.5:n.935A>T
ENST00000491488.5:n.110-1851A>T
ENST00000493368.5:n.440A>T
ENST00000607784.1:c.383A>T	ENSP00000475569.1:p.Glu128Val
NM_012203.1:c.383A>T	NP_036335.1:p.Glu128Val
XM_005251631.1:c.84-1851A>T	XP_005251688.1:n.84-1851A>T
XM_011518073.1:c.-380A>T	XP_011516375.1:n.-380A>T
XR_929374.1:n.468A>T
XM_017015320.2:c.383A>T	XP_016870809.1:p.Glu128Val
XM_017015321.2:c.383A>T	XP_016870810.1:p.Glu128Val
XM_017015323.2:c.-380A>T	XP_016870812.1:n.-380A>T
XM_024447716.1:c.656A>T	XP_024303484.1:p.Glu219Val
XM_024447717.1:c.656A>T	XP_024303485.1:p.Glu219Val
XR_002956828.1:n.671A>T
XR_002956829.1:n.671A>T
XR_002956830.1:n.442A>T
XR_002956831.1:n.139-1851A>T
XR_002956832.1:n.442A>T
NM_012203.2:c.383A>T MANE Select	NP_036335.1:p.Glu128Val