Canonical Allele Identifier: CA1846866317
Gene: GRHPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37426537G= , CM000671.2:g.37426537G= GRCh38
NC_000009.11:g.37426534G= , CM000671.1:g.37426534G= GRCh37
NC_000009.10:g.37416534G= NCBI36
NG_008135.1:g.8828G=

Transcript Alleles

HGVS Amino-acid change
ENST00000318158.11:c.288-1G= MANE Select ENSP00000313432.6:n.288-1G=
ENST00000318158.10:c.288-1G= ENSP00000313432.6:n.288-1G=
ENST00000377824.8:n.325-1G=
ENST00000460882.5:n.315-1G=
ENST00000487399.5:n.839G=
ENST00000491488.5:n.110-1947G=
ENST00000493368.5:n.345-1G=
ENST00000607784.1:c.288-1G= ENSP00000475569.1:n.288-1G=
NM_012203.1:c.288-1G= NP_036335.1:n.288-1G=
XM_005251631.1:c.84-1947G= XP_005251688.1:n.84-1947G=
XM_011518073.1:c.-475-1G= XP_011516375.1:n.-475-1G=
XR_929374.1:n.373-1G=
XM_017015320.2:c.288-1G= XP_016870809.1:n.288-1G=
XM_017015321.2:c.288-1G= XP_016870810.1:n.288-1G=
XM_017015323.2:c.-475-1G= XP_016870812.1:n.-475-1G=
XM_024447716.1:c.561-1G= XP_024303484.1:n.561-1G=
XM_024447717.1:c.561-1G= XP_024303485.1:n.561-1G=
XR_002956828.1:n.576-1G=
XR_002956829.1:n.576-1G=
XR_002956830.1:n.347-1G=
XR_002956831.1:n.139-1947G=
XR_002956832.1:n.347-1G=
NM_012203.2:c.288-1G= MANE Select NP_036335.1:n.288-1G=