Canonical Allele Identifier: CA1846864944
Gene: GRHPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37424915G= , CM000671.2:g.37424915G= GRCh38
NC_000009.11:g.37424912G= , CM000671.1:g.37424912G= GRCh37
NC_000009.10:g.37414912G= NCBI36
NG_008135.1:g.7206G=

Transcript Alleles

HGVS Amino-acid change
ENST00000318158.11:c.154G= MANE Select ENSP00000313432.6:p.Ala52=
ENST00000318158.10:c.154G= ENSP00000313432.6:p.Ala52=
ENST00000377824.8:n.191G=
ENST00000460882.5:n.181G=
ENST00000487399.5:n.163G=
ENST00000491488.5:n.109+2082G=
ENST00000493368.5:n.211G=
ENST00000607784.1:c.154G= ENSP00000475569.1:p.Ala52=
NM_012203.1:c.154G= NP_036335.1:p.Ala52=
XM_005251631.1:c.83+2082G= XP_005251688.1:n.83+2082G=
XM_011518073.1:c.-609G= XP_011516375.1:n.-609G=
XR_929374.1:n.239G=
XM_017015320.2:c.154G= XP_016870809.1:p.Ala52=
XM_017015321.2:c.154G= XP_016870810.1:p.Ala52=
XM_017015323.2:c.-609G= XP_016870812.1:n.-609G=
XM_024447716.1:c.427G= XP_024303484.1:p.Ala143=
XM_024447717.1:c.427G= XP_024303485.1:p.Ala143=
XR_002956828.1:n.442G=
XR_002956829.1:n.442G=
XR_002956830.1:n.213G=
XR_002956831.1:n.138+2082G=
XR_002956832.1:n.213G=
NM_012203.2:c.154G= MANE Select NP_036335.1:p.Ala52=