Canonical Allele Identifier: CA2689952862
Gene: GRHPR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37425893_37425894insGG , CM000671.2:g.37425893_37425894insGG GRCh38
NC_000009.11:g.37425890_37425891insGG , CM000671.1:g.37425890_37425891insGG GRCh37
NC_000009.10:g.37415890_37415891insGG NCBI36
NG_008135.1:g.8184_8185insGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000318158.11:c.215-29_215-28insGG MANE Select ENSP00000313432.6:n.215-29_215-28insGG
ENST00000318158.10:c.215-29_215-28insGG ENSP00000313432.6:n.215-29_215-28insGG
ENST00000377824.8:n.252-29_252-28insGG
ENST00000460882.5:n.242-29_242-28insGG
ENST00000487399.5:n.224-29_224-28insGG
ENST00000491488.5:n.110-2591_110-2590insGG
ENST00000493368.5:n.272-29_272-28insGG
ENST00000607784.1:c.215-29_215-28insGG ENSP00000475569.1:n.215-29_215-28insGG
NM_012203.1:c.215-29_215-28insGG NP_036335.1:n.215-29_215-28insGG
XM_005251631.1:c.84-2591_84-2590insGG XP_005251688.1:n.84-2591_84-2590insGG
XM_011518073.1:c.-548-29_-548-28insGG XP_011516375.1:n.-548-29_-548-28insGG
XR_929374.1:n.300-29_300-28insGG
XM_017015320.2:c.215-29_215-28insGG XP_016870809.1:n.215-29_215-28insGG
XM_017015321.2:c.215-29_215-28insGG XP_016870810.1:n.215-29_215-28insGG
XM_017015323.2:c.-548-29_-548-28insGG XP_016870812.1:n.-548-29_-548-28insGG
XM_024447716.1:c.488-29_488-28insGG XP_024303484.1:n.488-29_488-28insGG
XM_024447717.1:c.488-29_488-28insGG XP_024303485.1:n.488-29_488-28insGG
XR_002956828.1:n.503-29_503-28insGG
XR_002956829.1:n.503-29_503-28insGG
XR_002956830.1:n.274-29_274-28insGG
XR_002956831.1:n.139-2591_139-2590insGG
XR_002956832.1:n.274-29_274-28insGG
NM_012203.2:c.215-29_215-28insGG MANE Select NP_036335.1:n.215-29_215-28insGG