Canonical Allele Identifier: CA5059056
Gene: GRHPR HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 371016
ClinVar RCV Id: RCV000411634

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37428533dup , CM000671.2:g.37428533dup GRCh38
NC_000009.11:g.37428530dup , CM000671.1:g.37428530dup GRCh37
NC_000009.10:g.37418530dup NCBI36
NG_008135.1:g.10824dup

Transcript Alleles

HGVS Amino-acid change
NM_012203.1:c.454dup VV NP_036335.1:p.Thr152AsnfsTer?
XM_005251631.1:c.133dup XP_005251688.1:p.Thr45AsnfsTer?
XM_011518073.1:c.-309dup XP_011516375.1:p.=
XR_929374.1:n.539dup
XM_017015320.2:c.454dup XP_016870809.1:p.Thr152AsnfsTer?
XM_017015321.2:c.454dup XP_016870810.1:p.Thr152AsnfsTer?
XM_017015323.2:c.-309dup XP_016870812.1:p.=
XM_024447716.1:c.727dup XP_024303484.1:p.Thr243AsnfsTer?
XM_024447717.1:c.727dup XP_024303485.1:p.Thr243AsnfsTer?
XR_002956828.1:n.742dup
XR_002956829.1:n.742dup
XR_002956830.1:n.513dup
XR_002956831.1:n.188dup
XR_002956832.1:n.513dup
ENST00000318158.10:c.454dup ENSP00000313432.6:p.Thr152AsnfsTer?
ENST00000377824.8:n.491dup
ENST00000460882.5:n.481dup
ENST00000491488.5:n.159dup
ENST00000493368.5:n.511dup
ENST00000497693.1:n.828dup
ENST00000607784.1:c.454dup ENSP00000475569.1:p.Thr152AsnfsTer?