Canonical Allele Identifier: CA1846868742
Gene: GRHPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37428327A= , CM000671.2:g.37428327A= GRCh38
NC_000009.11:g.37428324A= , CM000671.1:g.37428324A= GRCh37
NC_000009.10:g.37418324A= NCBI36
NG_008135.1:g.10618A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318158.11:c.405-157A= MANE Select ENSP00000313432.6:n.405-157A=
ENST00000318158.10:c.405-157A= ENSP00000313432.6:n.405-157A=
ENST00000377824.8:n.442-157A=
ENST00000460882.5:n.432-157A=
ENST00000491488.5:n.110-157A=
ENST00000493368.5:n.462-157A=
ENST00000497693.1:n.622A=
ENST00000607784.1:c.405-157A= ENSP00000475569.1:n.405-157A=
NM_012203.1:c.405-157A= NP_036335.1:n.405-157A=
XM_005251631.1:c.84-157A= XP_005251688.1:n.84-157A=
XM_011518073.1:c.-358-157A= XP_011516375.1:n.-358-157A=
XR_929374.1:n.490-157A=
XM_017015320.2:c.405-157A= XP_016870809.1:n.405-157A=
XM_017015321.2:c.405-157A= XP_016870810.1:n.405-157A=
XM_017015323.2:c.-358-157A= XP_016870812.1:n.-358-157A=
XM_024447716.1:c.678-157A= XP_024303484.1:n.678-157A=
XM_024447717.1:c.678-157A= XP_024303485.1:n.678-157A=
XR_002956828.1:n.693-157A=
XR_002956829.1:n.693-157A=
XR_002956830.1:n.464-157A=
XR_002956831.1:n.139-157A=
XR_002956832.1:n.464-157A=
NM_012203.2:c.405-157A= MANE Select NP_036335.1:n.405-157A=