Canonical Allele Identifier: CA2783586062
Gene: GRHPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37428324_37428325insGAA , CM000671.2:g.37428324_37428325insGAA GRCh38
NC_000009.11:g.37428321_37428322insGAA , CM000671.1:g.37428321_37428322insGAA GRCh37
NC_000009.10:g.37418321_37418322insGAA NCBI36
NG_008135.1:g.10615_10616insGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000318158.11:c.405-160_405-159insGAA MANE Select ENSP00000313432.6:n.405-160_405-159insGAA
ENST00000318158.10:c.405-160_405-159insGAA ENSP00000313432.6:n.405-160_405-159insGAA
ENST00000377824.8:n.442-160_442-159insGAA
ENST00000460882.5:n.432-160_432-159insGAA
ENST00000491488.5:n.110-160_110-159insGAA
ENST00000493368.5:n.462-160_462-159insGAA
ENST00000497693.1:n.619_620insGAA
ENST00000607784.1:c.405-160_405-159insGAA ENSP00000475569.1:n.405-160_405-159insGAA
NM_012203.1:c.405-160_405-159insGAA NP_036335.1:n.405-160_405-159insGAA
XM_005251631.1:c.84-160_84-159insGAA XP_005251688.1:n.84-160_84-159insGAA
XM_011518073.1:c.-358-160_-358-159insGAA XP_011516375.1:n.-358-160_-358-159insGAA
XR_929374.1:n.490-160_490-159insGAA
XM_017015320.2:c.405-160_405-159insGAA XP_016870809.1:n.405-160_405-159insGAA
XM_017015321.2:c.405-160_405-159insGAA XP_016870810.1:n.405-160_405-159insGAA
XM_017015323.2:c.-358-160_-358-159insGAA XP_016870812.1:n.-358-160_-358-159insGAA
XM_024447716.1:c.678-160_678-159insGAA XP_024303484.1:n.678-160_678-159insGAA
XM_024447717.1:c.678-160_678-159insGAA XP_024303485.1:n.678-160_678-159insGAA
XR_002956828.1:n.693-160_693-159insGAA
XR_002956829.1:n.693-160_693-159insGAA
XR_002956830.1:n.464-160_464-159insGAA
XR_002956831.1:n.139-160_139-159insGAA
XR_002956832.1:n.464-160_464-159insGAA
NM_012203.2:c.405-160_405-159insGAA MANE Select NP_036335.1:n.405-160_405-159insGAA