Canonical Allele Identifier: CA2783586064
Gene: GRHPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37428325_37428326insGGGGG , CM000671.2:g.37428325_37428326insGGGGG GRCh38
NC_000009.11:g.37428322_37428323insGGGGG , CM000671.1:g.37428322_37428323insGGGGG GRCh37
NC_000009.10:g.37418322_37418323insGGGGG NCBI36
NG_008135.1:g.10616_10617insGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000318158.11:c.405-159_405-158insGGGGG MANE Select ENSP00000313432.6:n.405-159_405-158insGGGGG
ENST00000318158.10:c.405-159_405-158insGGGGG ENSP00000313432.6:n.405-159_405-158insGGGGG
ENST00000377824.8:n.442-159_442-158insGGGGG
ENST00000460882.5:n.432-159_432-158insGGGGG
ENST00000491488.5:n.110-159_110-158insGGGGG
ENST00000493368.5:n.462-159_462-158insGGGGG
ENST00000497693.1:n.620_621insGGGGG
ENST00000607784.1:c.405-159_405-158insGGGGG ENSP00000475569.1:n.405-159_405-158insGGGGG
NM_012203.1:c.405-159_405-158insGGGGG NP_036335.1:n.405-159_405-158insGGGGG
XM_005251631.1:c.84-159_84-158insGGGGG XP_005251688.1:n.84-159_84-158insGGGGG
XM_011518073.1:c.-358-159_-358-158insGGGGG XP_011516375.1:n.-358-159_-358-158insGGGGG
XR_929374.1:n.490-159_490-158insGGGGG
XM_017015320.2:c.405-159_405-158insGGGGG XP_016870809.1:n.405-159_405-158insGGGGG
XM_017015321.2:c.405-159_405-158insGGGGG XP_016870810.1:n.405-159_405-158insGGGGG
XM_017015323.2:c.-358-159_-358-158insGGGGG XP_016870812.1:n.-358-159_-358-158insGGGGG
XM_024447716.1:c.678-159_678-158insGGGGG XP_024303484.1:n.678-159_678-158insGGGGG
XM_024447717.1:c.678-159_678-158insGGGGG XP_024303485.1:n.678-159_678-158insGGGGG
XR_002956828.1:n.693-159_693-158insGGGGG
XR_002956829.1:n.693-159_693-158insGGGGG
XR_002956830.1:n.464-159_464-158insGGGGG
XR_002956831.1:n.139-159_139-158insGGGGG
XR_002956832.1:n.464-159_464-158insGGGGG
NM_012203.2:c.405-159_405-158insGGGGG MANE Select NP_036335.1:n.405-159_405-158insGGGGG