Canonical Allele Identifier: CA2742040164

Gene: GRHPR

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436635_37436637delinsCCT , CM000671.2:g.37436635_37436637delinsCCT	GRCh38
NC_000009.11:g.37436632_37436634delinsCCT , CM000671.1:g.37436632_37436634delinsCCT	GRCh37
NC_000009.10:g.37426632_37426634delinsCCT	NCBI36
NG_008135.1:g.18926_18928delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.866-26_866-24delinsCCT MANE Select	ENSP00000313432.6:n.866-26_866-24delinsCCT
ENST00000318158.10:c.866-26_866-24delinsCCT	ENSP00000313432.6:n.866-26_866-24delinsCCT
ENST00000460882.5:n.893-26_893-24delinsCCT
ENST00000480596.5:n.1567-26_1567-24delinsCCT
ENST00000491488.5:n.571-26_571-24delinsCCT
ENST00000494290.1:c.*52-246_*52-244delinsCCT	ENSP00000432021.1:n.*52-246_*52-244delinsCCT
ENST00000497693.1:n.4434-26_4434-24delinsCCT
NM_012203.1:c.866-26_866-24delinsCCT	NP_036335.1:n.866-26_866-24delinsCCT
XM_005251631.1:c.545-26_545-24delinsCCT	XP_005251688.1:n.545-26_545-24delinsCCT
XM_011518073.1:c.464-26_464-24delinsCCT	XP_011516375.1:n.464-26_464-24delinsCCT
XM_017015320.2:c.946-776_946-774delinsCCT	XP_016870809.1:n.946-776_946-774delinsCCT
XM_017015321.2:c.866-776_866-774delinsCCT	XP_016870810.1:n.866-776_866-774delinsCCT
XM_017015323.2:c.544-776_544-774delinsCCT	XP_016870812.1:n.544-776_544-774delinsCCT
XM_024447716.1:c.1219-776_1219-774delinsCCT	XP_024303484.1:n.1219-776_1219-774delinsCCT
XM_024447717.1:c.1139-776_1139-774delinsCCT	XP_024303485.1:n.1139-776_1139-774delinsCCT
XR_002956828.1:n.1234-776_1234-774delinsCCT
XR_002956829.1:n.1154-776_1154-774delinsCCT
XR_002956830.1:n.2286-26_2286-24delinsCCT
XR_002956831.1:n.1961-26_1961-24delinsCCT
XR_002956832.1:n.1285-26_1285-24delinsCCT
NM_012203.2:c.866-26_866-24delinsCCT MANE Select	NP_036335.1:n.866-26_866-24delinsCCT