Canonical Allele Identifier: CA1846864773
Gene: GRHPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37424816T= , CM000671.2:g.37424816T= GRCh38
NC_000009.11:g.37424813T= , CM000671.1:g.37424813T= GRCh37
NC_000009.10:g.37414813T= NCBI36
NG_008135.1:g.7107T=

Transcript Alleles

HGVS Amino-acid change
ENST00000318158.11:c.84-29T= MANE Select ENSP00000313432.6:n.84-29T=
ENST00000318158.10:c.84-29T= ENSP00000313432.6:n.84-29T=
ENST00000377824.8:n.121-29T=
ENST00000460882.5:n.111-29T=
ENST00000487399.5:n.93-29T=
ENST00000491488.5:n.109+1983T=
ENST00000493368.5:n.141-29T=
ENST00000607784.1:c.84-29T= ENSP00000475569.1:n.84-29T=
NM_012203.1:c.84-29T= NP_036335.1:n.84-29T=
XM_005251631.1:c.83+1983T= XP_005251688.1:n.83+1983T=
XM_011518073.1:c.-679-29T= XP_011516375.1:n.-679-29T=
XR_929374.1:n.169-29T=
XM_017015320.2:c.84-29T= XP_016870809.1:n.84-29T=
XM_017015321.2:c.84-29T= XP_016870810.1:n.84-29T=
XM_017015323.2:c.-679-29T= XP_016870812.1:n.-679-29T=
XM_024447716.1:c.357-29T= XP_024303484.1:n.357-29T=
XM_024447717.1:c.357-29T= XP_024303485.1:n.357-29T=
XR_002956828.1:n.372-29T=
XR_002956829.1:n.372-29T=
XR_002956830.1:n.143-29T=
XR_002956831.1:n.138+1983T=
XR_002956832.1:n.143-29T=
NM_012203.2:c.84-29T= MANE Select NP_036335.1:n.84-29T=