Canonical Allele Identifier: CA373442953
Gene: GRHPR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37429734C>A , CM000671.2:g.37429734C>A GRCh38
NC_000009.11:g.37429731C>A , CM000671.1:g.37429731C>A GRCh37
NC_000009.10:g.37419731C>A NCBI36
NG_008135.1:g.12025C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318158.11:c.496C>A MANE Select ENSP00000313432.6:p.Gln166Lys
ENST00000318158.10:c.496C>A ENSP00000313432.6:p.Gln166Lys
ENST00000377824.8:n.533C>A
ENST00000460882.5:n.523C>A
ENST00000480596.5:n.1197C>A
ENST00000491488.5:n.201C>A
ENST00000494290.1:c.67C>A ENSP00000432021.1:p.Gln23Lys
ENST00000497693.1:n.2029C>A
ENST00000607784.1:c.496C>A ENSP00000475569.1:p.Gln166Lys
NM_012203.1:c.496C>A NP_036335.1:p.Gln166Lys
XM_005251631.1:c.175C>A XP_005251688.1:p.Gln59Lys
XM_011518073.1:c.94C>A XP_011516375.1:p.Gln32Lys
XR_929374.1:n.941C>A
XM_017015320.2:c.496C>A XP_016870809.1:p.Gln166Lys
XM_017015321.2:c.496C>A XP_016870810.1:p.Gln166Lys
XM_017015323.2:c.94C>A XP_016870812.1:p.Gln32Lys
XM_024447716.1:c.769C>A XP_024303484.1:p.Gln257Lys
XM_024447717.1:c.769C>A XP_024303485.1:p.Gln257Lys
XR_002956828.1:n.784C>A
XR_002956829.1:n.784C>A
XR_002956830.1:n.555C>A
XR_002956831.1:n.230C>A
XR_002956832.1:n.915C>A
NM_012203.2:c.496C>A MANE Select NP_036335.1:p.Gln166Lys