Canonical Allele Identifier: CA2689954504
Gene: GRHPR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37428475_37428476dup , CM000671.2:g.37428475_37428476dup GRCh38
NC_000009.11:g.37428472_37428473dup , CM000671.1:g.37428472_37428473dup GRCh37
NC_000009.10:g.37418472_37418473dup NCBI36
NG_008135.1:g.10766_10767dup

Transcript Alleles

HGVS Amino-acid change
ENST00000318158.11:c.405-9_405-8dup MANE Select ENSP00000313432.6:n.405-9_405-8dup
ENST00000318158.10:c.405-9_405-8dup ENSP00000313432.6:n.405-9_405-8dup
ENST00000377824.8:n.442-9_442-8dup
ENST00000460882.5:n.432-9_432-8dup
ENST00000491488.5:n.110-9_110-8dup
ENST00000493368.5:n.462-9_462-8dup
ENST00000497693.1:n.770_771dup
ENST00000607784.1:c.405-9_405-8dup ENSP00000475569.1:n.405-9_405-8dup
NM_012203.1:c.405-9_405-8dup NP_036335.1:n.405-9_405-8dup
XM_005251631.1:c.84-9_84-8dup XP_005251688.1:n.84-9_84-8dup
XM_011518073.1:c.-358-9_-358-8dup XP_011516375.1:n.-358-9_-358-8dup
XR_929374.1:n.490-9_490-8dup
XM_017015320.2:c.405-9_405-8dup XP_016870809.1:n.405-9_405-8dup
XM_017015321.2:c.405-9_405-8dup XP_016870810.1:n.405-9_405-8dup
XM_017015323.2:c.-358-9_-358-8dup XP_016870812.1:n.-358-9_-358-8dup
XM_024447716.1:c.678-9_678-8dup XP_024303484.1:n.678-9_678-8dup
XM_024447717.1:c.678-9_678-8dup XP_024303485.1:n.678-9_678-8dup
XR_002956828.1:n.693-9_693-8dup
XR_002956829.1:n.693-9_693-8dup
XR_002956830.1:n.464-9_464-8dup
XR_002956831.1:n.139-9_139-8dup
XR_002956832.1:n.464-9_464-8dup
NM_012203.2:c.405-9_405-8dup MANE Select NP_036335.1:n.405-9_405-8dup