Canonical Allele Identifier: CA2689981329
Gene: GRHPR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37429799del , CM000671.2:g.37429799del GRCh38
NC_000009.11:g.37429796del , CM000671.1:g.37429796del GRCh37
NC_000009.10:g.37419796del NCBI36
NG_008135.1:g.12090del

Transcript Alleles

HGVS Amino-acid Change
ENST00000318158.11:c.561del MANE Select ENSP00000313432.6:p.Arg188GlyfsTer?
ENST00000318158.10:c.561del ENSP00000313432.6:p.Arg188GlyfsTer?
ENST00000377824.8:n.598del
ENST00000460882.5:n.588del
ENST00000480596.5:n.1262del
ENST00000482603.1:n.14del
ENST00000491488.5:n.266del
ENST00000494290.1:c.132del ENSP00000432021.1:p.Arg45GlyfsTer?
ENST00000497693.1:n.2094del
ENST00000607784.1:c.561del ENSP00000475569.1:p.Arg188GlyfsTer?
NM_012203.1:c.561del NP_036335.1:p.Arg188GlyfsTer?
XM_005251631.1:c.240del XP_005251688.1:p.Arg81GlyfsTer?
XM_011518073.1:c.159del XP_011516375.1:p.Arg54GlyfsTer?
XR_929374.1:n.1006del
XM_017015320.2:c.561del XP_016870809.1:p.Arg188GlyfsTer?
XM_017015321.2:c.561del XP_016870810.1:p.Arg188GlyfsTer?
XM_017015323.2:c.159del XP_016870812.1:p.Arg54GlyfsTer?
XM_024447716.1:c.834del XP_024303484.1:p.Arg279GlyfsTer?
XM_024447717.1:c.834del XP_024303485.1:p.Arg279GlyfsTer?
XR_002956828.1:n.849del
XR_002956829.1:n.849del
XR_002956830.1:n.620del
XR_002956831.1:n.295del
XR_002956832.1:n.980del
NM_012203.2:c.561del MANE Select NP_036335.1:p.Arg188GlyfsTer?