Canonical Allele Identifier: CA1846870211
Gene: GRHPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37429558G= , CM000671.2:g.37429558G= GRCh38
NC_000009.11:g.37429555G= , CM000671.1:g.37429555G= GRCh37
NC_000009.10:g.37419555G= NCBI36
NG_008135.1:g.11849G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318158.11:c.494-174G= MANE Select ENSP00000313432.6:n.494-174G=
ENST00000318158.10:c.494-174G= ENSP00000313432.6:n.494-174G=
ENST00000377824.8:n.531-174G=
ENST00000460882.5:n.521-174G=
ENST00000480596.5:n.1021G=
ENST00000491488.5:n.199-174G=
ENST00000494290.1:c.-110G= ENSP00000432021.1:n.-110G=
ENST00000497693.1:n.1853G=
ENST00000607784.1:c.494-174G= ENSP00000475569.1:n.494-174G=
NM_012203.1:c.494-174G= NP_036335.1:n.494-174G=
XM_005251631.1:c.173-174G= XP_005251688.1:n.173-174G=
XM_011518073.1:c.92-174G= XP_011516375.1:n.92-174G=
XR_929374.1:n.939-174G=
XM_017015320.2:c.494-174G= XP_016870809.1:n.494-174G=
XM_017015321.2:c.494-174G= XP_016870810.1:n.494-174G=
XM_017015323.2:c.92-174G= XP_016870812.1:n.92-174G=
XM_024447716.1:c.767-174G= XP_024303484.1:n.767-174G=
XM_024447717.1:c.767-174G= XP_024303485.1:n.767-174G=
XR_002956828.1:n.782-174G=
XR_002956829.1:n.782-174G=
XR_002956830.1:n.553-174G=
XR_002956831.1:n.228-174G=
XR_002956832.1:n.913-174G=
NM_012203.2:c.494-174G= MANE Select NP_036335.1:n.494-174G=