Canonical Allele Identifier: CA1846870521
Gene: GRHPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37429774G= , CM000671.2:g.37429774G= GRCh38
NC_000009.11:g.37429771G= , CM000671.1:g.37429771G= GRCh37
NC_000009.10:g.37419771G= NCBI36
NG_008135.1:g.12065G=

Transcript Alleles

HGVS Amino-acid change
ENST00000318158.11:c.536G= MANE Select ENSP00000313432.6:p.Arg179=
ENST00000318158.10:c.536G= ENSP00000313432.6:p.Arg179=
ENST00000377824.8:n.573G=
ENST00000460882.5:n.563G=
ENST00000480596.5:n.1237G=
ENST00000491488.5:n.241G=
ENST00000494290.1:c.107G= ENSP00000432021.1:p.Arg36=
ENST00000497693.1:n.2069G=
ENST00000607784.1:c.536G= ENSP00000475569.1:p.Arg179=
NM_012203.1:c.536G= NP_036335.1:p.Arg179=
XM_005251631.1:c.215G= XP_005251688.1:p.Arg72=
XM_011518073.1:c.134G= XP_011516375.1:p.Arg45=
XR_929374.1:n.981G=
XM_017015320.2:c.536G= XP_016870809.1:p.Arg179=
XM_017015321.2:c.536G= XP_016870810.1:p.Arg179=
XM_017015323.2:c.134G= XP_016870812.1:p.Arg45=
XM_024447716.1:c.809G= XP_024303484.1:p.Arg270=
XM_024447717.1:c.809G= XP_024303485.1:p.Arg270=
XR_002956828.1:n.824G=
XR_002956829.1:n.824G=
XR_002956830.1:n.595G=
XR_002956831.1:n.270G=
XR_002956832.1:n.955G=
NM_012203.2:c.536G= MANE Select NP_036335.1:p.Arg179=