Canonical Allele Identifier: CA1846865662
Gene: GRHPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37425860C= , CM000671.2:g.37425860C= GRCh38
NC_000009.11:g.37425857C= , CM000671.1:g.37425857C= GRCh37
NC_000009.10:g.37415857C= NCBI36
NG_008135.1:g.8151C=

Transcript Alleles

HGVS Amino-acid change
ENST00000318158.11:c.215-62C= MANE Select ENSP00000313432.6:n.215-62C=
ENST00000318158.10:c.215-62C= ENSP00000313432.6:n.215-62C=
ENST00000377824.8:n.252-62C=
ENST00000460882.5:n.242-62C=
ENST00000487399.5:n.224-62C=
ENST00000491488.5:n.110-2624C=
ENST00000493368.5:n.272-62C=
ENST00000607784.1:c.215-62C= ENSP00000475569.1:n.215-62C=
NM_012203.1:c.215-62C= NP_036335.1:n.215-62C=
XM_005251631.1:c.84-2624C= XP_005251688.1:n.84-2624C=
XM_011518073.1:c.-548-62C= XP_011516375.1:n.-548-62C=
XR_929374.1:n.300-62C=
XM_017015320.2:c.215-62C= XP_016870809.1:n.215-62C=
XM_017015321.2:c.215-62C= XP_016870810.1:n.215-62C=
XM_017015323.2:c.-548-62C= XP_016870812.1:n.-548-62C=
XM_024447716.1:c.488-62C= XP_024303484.1:n.488-62C=
XM_024447717.1:c.488-62C= XP_024303485.1:n.488-62C=
XR_002956828.1:n.503-62C=
XR_002956829.1:n.503-62C=
XR_002956830.1:n.274-62C=
XR_002956831.1:n.139-2624C=
XR_002956832.1:n.274-62C=
NM_012203.2:c.215-62C= MANE Select NP_036335.1:n.215-62C=