Canonical Allele Identifier: CA1846885218
Gene: GRHPR HGNC NCBI

Linked Data

dbSNP Id: rs1823663161

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37436603_37436627del , CM000671.2:g.37436603_37436627del GRCh38
NC_000009.11:g.37436600_37436624del , CM000671.1:g.37436600_37436624del GRCh37
NC_000009.10:g.37426600_37426624del NCBI36
NG_008135.1:g.18894_18918del

Transcript Alleles

HGVS Amino-acid Change
ENST00000318158.11:c.866-58_866-34del MANE Select ENSP00000313432.6:n.866-58_866-34del
ENST00000318158.10:c.866-58_866-34del ENSP00000313432.6:n.866-58_866-34del
ENST00000460882.5:n.893-58_893-34del
ENST00000480596.5:n.1567-58_1567-34del
ENST00000491488.5:n.571-58_571-34del
ENST00000494290.1:c.*52-278_*52-254del ENSP00000432021.1:n.*52-278_*52-254del
ENST00000497693.1:n.4434-58_4434-34del
NM_012203.1:c.866-58_866-34del NP_036335.1:n.866-58_866-34del
XM_005251631.1:c.545-58_545-34del XP_005251688.1:n.545-58_545-34del
XM_011518073.1:c.464-58_464-34del XP_011516375.1:n.464-58_464-34del
XM_017015320.2:c.946-808_946-784del XP_016870809.1:n.946-808_946-784del
XM_017015321.2:c.866-808_866-784del XP_016870810.1:n.866-808_866-784del
XM_017015323.2:c.544-808_544-784del XP_016870812.1:n.544-808_544-784del
XM_024447716.1:c.1219-808_1219-784del XP_024303484.1:n.1219-808_1219-784del
XM_024447717.1:c.1139-808_1139-784del XP_024303485.1:n.1139-808_1139-784del
XR_002956828.1:n.1234-808_1234-784del
XR_002956829.1:n.1154-808_1154-784del
XR_002956830.1:n.2286-58_2286-34del
XR_002956831.1:n.1961-58_1961-34del
XR_002956832.1:n.1285-58_1285-34del
NM_012203.2:c.866-58_866-34del MANE Select NP_036335.1:n.866-58_866-34del