Canonical Allele Identifier: CA2783585974
Gene: GRHPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37426529_37426531del , CM000671.2:g.37426529_37426531del GRCh38
NC_000009.11:g.37426526_37426528del , CM000671.1:g.37426526_37426528del GRCh37
NC_000009.10:g.37416526_37416528del NCBI36
NG_008135.1:g.8820_8822del

Transcript Alleles

HGVS Amino-acid Change
ENST00000318158.11:c.288-9_288-7del MANE Select ENSP00000313432.6:n.288-9_288-7del
ENST00000318158.10:c.288-9_288-7del ENSP00000313432.6:n.288-9_288-7del
ENST00000377824.8:n.325-9_325-7del
ENST00000460882.5:n.315-9_315-7del
ENST00000487399.5:n.831_833del
ENST00000491488.5:n.110-1955_110-1953del
ENST00000493368.5:n.345-9_345-7del
ENST00000607784.1:c.288-9_288-7del ENSP00000475569.1:n.288-9_288-7del
NM_012203.1:c.288-9_288-7del NP_036335.1:n.288-9_288-7del
XM_005251631.1:c.84-1955_84-1953del XP_005251688.1:n.84-1955_84-1953del
XM_011518073.1:c.-475-9_-475-7del XP_011516375.1:n.-475-9_-475-7del
XR_929374.1:n.373-9_373-7del
XM_017015320.2:c.288-9_288-7del XP_016870809.1:n.288-9_288-7del
XM_017015321.2:c.288-9_288-7del XP_016870810.1:n.288-9_288-7del
XM_017015323.2:c.-475-9_-475-7del XP_016870812.1:n.-475-9_-475-7del
XM_024447716.1:c.561-9_561-7del XP_024303484.1:n.561-9_561-7del
XM_024447717.1:c.561-9_561-7del XP_024303485.1:n.561-9_561-7del
XR_002956828.1:n.576-9_576-7del
XR_002956829.1:n.576-9_576-7del
XR_002956830.1:n.347-9_347-7del
XR_002956831.1:n.139-1955_139-1953del
XR_002956832.1:n.347-9_347-7del
NM_012203.2:c.288-9_288-7del MANE Select NP_036335.1:n.288-9_288-7del