Canonical Allele Identifier: CA1846869021
Gene: GRHPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37428519G= , CM000671.2:g.37428519G= GRCh38
NC_000009.11:g.37428516G= , CM000671.1:g.37428516G= GRCh37
NC_000009.10:g.37418516G= NCBI36
NG_008135.1:g.10810G=

Transcript Alleles

HGVS Amino-acid change
ENST00000318158.11:c.440G= MANE Select ENSP00000313432.6:p.Cys147=
ENST00000318158.10:c.440G= ENSP00000313432.6:p.Cys147=
ENST00000377824.8:n.477G=
ENST00000460882.5:n.467G=
ENST00000491488.5:n.145G=
ENST00000493368.5:n.497G=
ENST00000497693.1:n.814G=
ENST00000607784.1:c.440G= ENSP00000475569.1:p.Cys147=
NM_012203.1:c.440G= NP_036335.1:p.Cys147=
XM_005251631.1:c.119G= XP_005251688.1:p.Cys40=
XM_011518073.1:c.-323G= XP_011516375.1:n.-323G=
XR_929374.1:n.525G=
XM_017015320.2:c.440G= XP_016870809.1:p.Cys147=
XM_017015321.2:c.440G= XP_016870810.1:p.Cys147=
XM_017015323.2:c.-323G= XP_016870812.1:n.-323G=
XM_024447716.1:c.713G= XP_024303484.1:p.Cys238=
XM_024447717.1:c.713G= XP_024303485.1:p.Cys238=
XR_002956828.1:n.728G=
XR_002956829.1:n.728G=
XR_002956830.1:n.499G=
XR_002956831.1:n.174G=
XR_002956832.1:n.499G=
NM_012203.2:c.440G= MANE Select NP_036335.1:p.Cys147=