Canonical Allele Identifier: CA1846866328
Gene: GRHPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37426540G= , CM000671.2:g.37426540G= GRCh38
NC_000009.11:g.37426537G= , CM000671.1:g.37426537G= GRCh37
NC_000009.10:g.37416537G= NCBI36
NG_008135.1:g.8831G=

Transcript Alleles

HGVS Amino-acid change
ENST00000318158.11:c.290G= MANE Select ENSP00000313432.6:p.Gly97=
ENST00000318158.10:c.290G= ENSP00000313432.6:p.Gly97=
ENST00000377824.8:n.327G=
ENST00000460882.5:n.317G=
ENST00000487399.5:n.842G=
ENST00000491488.5:n.110-1944G=
ENST00000493368.5:n.347G=
ENST00000607784.1:c.290G= ENSP00000475569.1:p.Gly97=
NM_012203.1:c.290G= NP_036335.1:p.Gly97=
XM_005251631.1:c.84-1944G= XP_005251688.1:n.84-1944G=
XM_011518073.1:c.-473G= XP_011516375.1:n.-473G=
XR_929374.1:n.375G=
XM_017015320.2:c.290G= XP_016870809.1:p.Gly97=
XM_017015321.2:c.290G= XP_016870810.1:p.Gly97=
XM_017015323.2:c.-473G= XP_016870812.1:n.-473G=
XM_024447716.1:c.563G= XP_024303484.1:p.Gly188=
XM_024447717.1:c.563G= XP_024303485.1:p.Gly188=
XR_002956828.1:n.578G=
XR_002956829.1:n.578G=
XR_002956830.1:n.349G=
XR_002956831.1:n.139-1944G=
XR_002956832.1:n.349G=
NM_012203.2:c.290G= MANE Select NP_036335.1:p.Gly97=