Canonical Allele Identifier: CA2689954120
Gene: GRHPR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37428325_37428326insAAA , CM000671.2:g.37428325_37428326insAAA GRCh38
NC_000009.11:g.37428322_37428323insAAA , CM000671.1:g.37428322_37428323insAAA GRCh37
NC_000009.10:g.37418322_37418323insAAA NCBI36
NG_008135.1:g.10616_10617insAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000318158.11:c.405-159_405-158insAAA MANE Select ENSP00000313432.6:n.405-159_405-158insAAA
ENST00000318158.10:c.405-159_405-158insAAA ENSP00000313432.6:n.405-159_405-158insAAA
ENST00000377824.8:n.442-159_442-158insAAA
ENST00000460882.5:n.432-159_432-158insAAA
ENST00000491488.5:n.110-159_110-158insAAA
ENST00000493368.5:n.462-159_462-158insAAA
ENST00000497693.1:n.620_621insAAA
ENST00000607784.1:c.405-159_405-158insAAA ENSP00000475569.1:n.405-159_405-158insAAA
NM_012203.1:c.405-159_405-158insAAA NP_036335.1:n.405-159_405-158insAAA
XM_005251631.1:c.84-159_84-158insAAA XP_005251688.1:n.84-159_84-158insAAA
XM_011518073.1:c.-358-159_-358-158insAAA XP_011516375.1:n.-358-159_-358-158insAAA
XR_929374.1:n.490-159_490-158insAAA
XM_017015320.2:c.405-159_405-158insAAA XP_016870809.1:n.405-159_405-158insAAA
XM_017015321.2:c.405-159_405-158insAAA XP_016870810.1:n.405-159_405-158insAAA
XM_017015323.2:c.-358-159_-358-158insAAA XP_016870812.1:n.-358-159_-358-158insAAA
XM_024447716.1:c.678-159_678-158insAAA XP_024303484.1:n.678-159_678-158insAAA
XM_024447717.1:c.678-159_678-158insAAA XP_024303485.1:n.678-159_678-158insAAA
XR_002956828.1:n.693-159_693-158insAAA
XR_002956829.1:n.693-159_693-158insAAA
XR_002956830.1:n.464-159_464-158insAAA
XR_002956831.1:n.139-159_139-158insAAA
XR_002956832.1:n.464-159_464-158insAAA
NM_012203.2:c.405-159_405-158insAAA MANE Select NP_036335.1:n.405-159_405-158insAAA