Canonical Allele Identifier: CA373442973

Gene: GRHPR

Linked Data

• MyVariant Identifiers: chr9:g.37429735C>G (hg19) ; chr9:g.37429738C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37429738C>G , CM000671.2:g.37429738C>G	GRCh38
NC_000009.11:g.37429735C>G , CM000671.1:g.37429735C>G	GRCh37
NC_000009.10:g.37419735C>G	NCBI36
NG_008135.1:g.12029C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.500C>G MANE Select	ENSP00000313432.6:p.Ala167Gly
ENST00000318158.10:c.500C>G	ENSP00000313432.6:p.Ala167Gly
ENST00000377824.8:n.537C>G
ENST00000460882.5:n.527C>G
ENST00000480596.5:n.1201C>G
ENST00000491488.5:n.205C>G
ENST00000494290.1:c.71C>G	ENSP00000432021.1:p.Ala24Gly
ENST00000497693.1:n.2033C>G
ENST00000607784.1:c.500C>G	ENSP00000475569.1:p.Ala167Gly
NM_012203.1:c.500C>G	NP_036335.1:p.Ala167Gly
XM_005251631.1:c.179C>G	XP_005251688.1:p.Ala60Gly
XM_011518073.1:c.98C>G	XP_011516375.1:p.Ala33Gly
XR_929374.1:n.945C>G
XM_017015320.2:c.500C>G	XP_016870809.1:p.Ala167Gly
XM_017015321.2:c.500C>G	XP_016870810.1:p.Ala167Gly
XM_017015323.2:c.98C>G	XP_016870812.1:p.Ala33Gly
XM_024447716.1:c.773C>G	XP_024303484.1:p.Ala258Gly
XM_024447717.1:c.773C>G	XP_024303485.1:p.Ala258Gly
XR_002956828.1:n.788C>G
XR_002956829.1:n.788C>G
XR_002956830.1:n.559C>G
XR_002956831.1:n.234C>G
XR_002956832.1:n.919C>G
NM_012203.2:c.500C>G MANE Select	NP_036335.1:p.Ala167Gly