Canonical Allele Identifier: CA373442823

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37428554G>C (hg19) ; chr9:g.37428557G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37428557G>C , CM000671.2:g.37428557G>C	GRCh38
NC_000009.11:g.37428554G>C , CM000671.1:g.37428554G>C	GRCh37
NC_000009.10:g.37418554G>C	NCBI36
NG_008135.1:g.10848G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.478G>C MANE Select	ENSP00000313432.6:p.Gly160Arg
ENST00000318158.10:c.478G>C	ENSP00000313432.6:p.Gly160Arg
ENST00000377824.8:n.515G>C
ENST00000460882.5:n.505G>C
ENST00000480596.5:n.20G>C
ENST00000491488.5:n.183G>C
ENST00000493368.5:n.535G>C
ENST00000497693.1:n.852G>C
ENST00000607784.1:c.478G>C	ENSP00000475569.1:p.Gly160Arg
NM_012203.1:c.478G>C	NP_036335.1:p.Gly160Arg
XM_005251631.1:c.157G>C	XP_005251688.1:p.Gly53Arg
XM_011518073.1:c.-285G>C	XP_011516375.1:n.-285G>C
XR_929374.1:n.563G>C
XM_017015320.2:c.478G>C	XP_016870809.1:p.Gly160Arg
XM_017015321.2:c.478G>C	XP_016870810.1:p.Gly160Arg
XM_017015323.2:c.-285G>C	XP_016870812.1:n.-285G>C
XM_024447716.1:c.751G>C	XP_024303484.1:p.Gly251Arg
XM_024447717.1:c.751G>C	XP_024303485.1:p.Gly251Arg
XR_002956828.1:n.766G>C
XR_002956829.1:n.766G>C
XR_002956830.1:n.537G>C
XR_002956831.1:n.212G>C
XR_002956832.1:n.537G>C
NM_012203.2:c.478G>C MANE Select	NP_036335.1:p.Gly160Arg