Canonical Allele Identifier: CA1846866619
Gene: GRHPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37426634G= , CM000671.2:g.37426634G= GRCh38
NC_000009.11:g.37426631G= , CM000671.1:g.37426631G= GRCh37
NC_000009.10:g.37416631G= NCBI36
NG_008135.1:g.8925G=

Transcript Alleles

HGVS Amino-acid change
ENST00000318158.11:c.384G= MANE Select ENSP00000313432.6:p.Glu128=
ENST00000318158.10:c.384G= ENSP00000313432.6:p.Glu128=
ENST00000377824.8:n.421G=
ENST00000460882.5:n.411G=
ENST00000487399.5:n.936G=
ENST00000491488.5:n.110-1850G=
ENST00000493368.5:n.441G=
ENST00000607784.1:c.384G= ENSP00000475569.1:p.Glu128=
NM_012203.1:c.384G= NP_036335.1:p.Glu128=
XM_005251631.1:c.84-1850G= XP_005251688.1:n.84-1850G=
XM_011518073.1:c.-379G= XP_011516375.1:n.-379G=
XR_929374.1:n.469G=
XM_017015320.2:c.384G= XP_016870809.1:p.Glu128=
XM_017015321.2:c.384G= XP_016870810.1:p.Glu128=
XM_017015323.2:c.-379G= XP_016870812.1:n.-379G=
XM_024447716.1:c.657G= XP_024303484.1:p.Glu219=
XM_024447717.1:c.657G= XP_024303485.1:p.Glu219=
XR_002956828.1:n.672G=
XR_002956829.1:n.672G=
XR_002956830.1:n.443G=
XR_002956831.1:n.139-1850G=
XR_002956832.1:n.443G=
NM_012203.2:c.384G= MANE Select NP_036335.1:p.Glu128=